WO2016093878A1 - Anti-cd70 chimeric antigen receptors - Google Patents

Anti-cd70 chimeric antigen receptors Download PDF

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Publication number
WO2016093878A1
WO2016093878A1 PCT/US2015/025047 US2015025047W WO2016093878A1 WO 2016093878 A1 WO2016093878 A1 WO 2016093878A1 US 2015025047 W US2015025047 W US 2015025047W WO 2016093878 A1 WO2016093878 A1 WO 2016093878A1
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Prior art keywords
amino acid
car
cells
seq
intracellular
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French (fr)
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Qiong J. Wang
Zhiya Yu
James C. Yang
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US Department of Health and Human Services
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US Department of Health and Human Services
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Priority to JP2017530742A priority Critical patent/JP6724009B2/ja
Priority to ES15718065T priority patent/ES2745153T3/es
Priority to EP15718065.4A priority patent/EP3230310B1/en
Priority to EP19178931.2A priority patent/EP3597663B1/en
Priority to CA2970280A priority patent/CA2970280A1/en
Priority to US15/531,626 priority patent/US10689456B2/en
Priority to CN201580066498.4A priority patent/CN107207616B/zh
Priority to SI201530869T priority patent/SI3230310T1/sl
Priority to PL15718065T priority patent/PL3230310T3/pl
Application filed by US Department of Health and Human Services filed Critical US Department of Health and Human Services
Priority to AU2015361261A priority patent/AU2015361261B2/en
Priority to EP22164990.8A priority patent/EP4043487A1/en
Publication of WO2016093878A1 publication Critical patent/WO2016093878A1/en
Anticipated expiration legal-status Critical
Priority to AU2020203836A priority patent/AU2020203836B2/en
Priority to US16/906,061 priority patent/US11999796B2/en
Priority to AU2021277627A priority patent/AU2021277627B2/en
Priority to US18/663,557 priority patent/US20240294665A1/en
Ceased legal-status Critical Current

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
    • C07K16/18—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
    • C07K16/28—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
    • C07K16/30—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants from tumour cells
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K40/00—Cellular immunotherapy
    • A61K40/10—Cellular immunotherapy characterised by the cell type used
    • A61K40/11—T-cells, e.g. tumour infiltrating lymphocytes [TIL] or regulatory T [Treg] cells; Lymphokine-activated killer [LAK] cells
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K40/00—Cellular immunotherapy
    • A61K40/30—Cellular immunotherapy characterised by the recombinant expression of specific molecules in the cells of the immune system
    • A61K40/31—Chimeric antigen receptors [CAR]
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K40/00—Cellular immunotherapy
    • A61K40/40—Cellular immunotherapy characterised by antigens that are targeted or presented by cells of the immune system
    • A61K40/41—Vertebrate antigens
    • A61K40/42—Cancer antigens
    • A61K40/4231—Cytokines
    • A61K40/4232—Tumor necrosis factors [TNF] or CD70
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • C—CHEMISTRY; METALLURGY
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    • C07K—PEPTIDES
    • C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • C07K14/705—Receptors; Cell surface antigens; Cell surface determinants
    • C07K14/70503—Immunoglobulin superfamily
    • C07K14/7051—T-cell receptor (TcR)-CD3 complex
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • C07K14/705—Receptors; Cell surface antigens; Cell surface determinants
    • C07K14/70503—Immunoglobulin superfamily
    • C07K14/70517—CD8
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • C07K14/705—Receptors; Cell surface antigens; Cell surface determinants
    • C07K14/70503—Immunoglobulin superfamily
    • C07K14/70521—CD28, CD152
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • C07K14/705—Receptors; Cell surface antigens; Cell surface determinants
    • C07K14/70578—NGF-receptor/TNF-receptor superfamily, e.g. CD27, CD30, CD40, CD95
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • C07K14/705—Receptors; Cell surface antigens; Cell surface determinants
    • C07K14/715—Receptors; Cell surface antigens; Cell surface determinants for cytokines; for lymphokines; for interferons
    • C07K14/7153—Receptors; Cell surface antigens; Cell surface determinants for cytokines; for lymphokines; for interferons for colony-stimulating factors [CSF]
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
    • C07K16/18—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
    • C07K16/28—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
    • C07K16/2875—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against the NGF/TNF superfamily, e.g. CD70, CD95L, CD153, CD154
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2239/00—Indexing codes associated with cellular immunotherapy of group A61K40/00
    • A61K2239/38—Indexing codes associated with cellular immunotherapy of group A61K40/00 characterised by the dose, timing or administration schedule
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2239/00—Indexing codes associated with cellular immunotherapy of group A61K40/00
    • A61K2239/46—Indexing codes associated with cellular immunotherapy of group A61K40/00 characterised by the cancer treated
    • A61K2239/57—Skin; melanoma
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K35/00—Medicinal preparations containing materials or reaction products thereof with undetermined constitution
    • A61K35/12—Materials from mammals; Compositions comprising non-specified tissues or cells; Compositions comprising non-embryonic stem cells; Genetically modified cells
    • A61K35/14—Blood; Artificial blood
    • A61K35/17—Lymphocytes; B-cells; T-cells; Natural killer cells; Interferon-activated or cytokine-activated lymphocytes
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2317/00—Immunoglobulins specific features
    • C07K2317/60—Immunoglobulins specific features characterized by non-natural combinations of immunoglobulin fragments
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2317/00—Immunoglobulins specific features
    • C07K2317/60—Immunoglobulins specific features characterized by non-natural combinations of immunoglobulin fragments
    • C07K2317/62—Immunoglobulins specific features characterized by non-natural combinations of immunoglobulin fragments comprising only variable region components
    • C07K2317/622—Single chain antibody (scFv)
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2319/00—Fusion polypeptide
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2319/00—Fusion polypeptide
    • C07K2319/01—Fusion polypeptide containing a localisation/targetting motif
    • C07K2319/02—Fusion polypeptide containing a localisation/targetting motif containing a signal sequence
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2319/00—Fusion polypeptide
    • C07K2319/01—Fusion polypeptide containing a localisation/targetting motif
    • C07K2319/03—Fusion polypeptide containing a localisation/targetting motif containing a transmembrane segment
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2319/00—Fusion polypeptide
    • C07K2319/33—Fusion polypeptide fusions for targeting to specific cell types, e.g. tissue specific targeting, targeting of a bacterial subspecies

Definitions

  • Cancer is a public health concern. Despite advances in treatments such as chemotherapy, the prognosis for many cancers, including renal cell carcinoma (RCC), glioblastoma, non-Hodgkin's lymphoma (NHL), chronic lymphocytic leukemia (CLL), diffuse large-B-cell lymphoma, and follicular lymphoma, may be poor. Accordingly, there exists an unmet need for additional treatments for cancer, particularly RCC, glioblastoma, NHL, CLL, diffuse large-B-cell lymphoma, and follicular lymphoma.
  • RCC renal cell carcinoma
  • NHL non-Hodgkin's lymphoma
  • CLL chronic lymphocytic leukemia
  • diffuse large-B-cell lymphoma and follicular lymphoma
  • An embodiment of the invention provides a chimeric antigen receptor (CAR) having antigenic specificity for CD70, the CAR comprising: an antigen binding - transmembrane domain comprising a CD27 amino acid sequence lacking all or a portion of the CD27 intracellular T cell signaling domain, wherein the portion is at least amino acid residues 237 to 260 as defined by SEQ ID NO: 2; a 4-1 BB intracellular T cell signaling domain; a CO3 intracellular T cell signaling domain; and optionally, a CD28 intracellular T cell signaling domain.
  • Another embodiment of the invention provides a CAR having antigenic specificity for CD70 comprising an amino acid sequence at least about 90% identical to any one of SEQ ID NOs: 1 1 -13.
  • Additional embodiments of the invention provide methods of detecting the presence of cancer in a mammal and methods of treating or preventing cancer in a mammal.
  • Figures 1 A and IB are graphs showing the tumor size (mm") of B16/mCD70- (A) or B16- (B) tumor bearing mice over a period of time (days) following administration of ⁇ 0 ⁇ 27-0 ⁇ 3 ⁇ CAR-transduced cells (closed circles), untransduced cells (open circles), phosphate buffered saline (PBS) (x), or pmel + VI (squares) and irradiation (500 Rads).
  • Figures 1C and ID are graphs showing the tumor size (mni ) of B16/mCD70- tumor bearing mice over a period of time (days) following administration of ⁇ 27-003 ⁇ CAR-transduced cells at a dose of 1 x 10 4 (T), 1 x 10 5 (closed squares), 1 x 10 6 (A), or 1 x 10 7 (closed circles) cells per mouse; PBS (open squares); cells transduced with an empty vector (open circles); or pmel + VI (diamonds) with (C) or without (D) irradiation (500 Rads).
  • Figure IE is a graph showing the survival (%) of Bl 6/mCD70-tumor bearing mice over a period of time (days) following administration of ⁇ 27- ⁇ 3 ⁇ CAR-transduced cells at a dose of 1 x 10 4 (diamonds), 1 x 10 5 (T), 1 x 10 6 (A), or 1 x 10 7 (closed circles) cells per mouse; PBS (open squares); cells transduced with an empty vector (open circles); or pmel + VI ( ⁇ ), followed by irradiation (500 Rads).
  • Figure I F is a graph showing the tumor size (mm ) of B16/mCD70-tumor bearing mice over a period of time (days) following administration of ⁇ 0 ⁇ 27 ⁇ 3 ⁇ CAR-transduced cells (squares), untransduced cells ( ⁇ ), cells transduced with an empty vector (V), or pmel + VI (circles), followed by irradiation and administration of IL-2.
  • Figures 2A-2D are graphs showing the average weight (g) of B 16/mCD70- (A and B) or B 16- (C and D) tumor bearing mice over a period of time (days) following
  • CAR-transduced cells closed circles
  • untransduced cells open squares
  • PBS phosphate buffered saline
  • V phosphate buffered saline
  • pmel + VI ⁇
  • Figures 2E-2H are graphs showing the absolute white blood cell count (K/ ⁇ ) (E and F) or splenocyte count (x 10 7 per spleen) (G and H) of B 16/mCD70-tumor bearing mice over a period of time (days) following administration of ⁇ 0 ⁇ 27-0 ⁇ 3 ⁇ CAR-transduced cells (cross-hatched bars), untransduced cells (unshaded bars), or cells transduced with a vector encoding green fluorescent protein (GFP) (diagonally striped bars) with (E and G) or without (F and H) irradiation (500 Rads).
  • K/ ⁇ E and F
  • splenocyte count x 10 7 per spleen
  • Figure 21 is a graph showing serum interferon (IFN) gamma (pg/ml) levels of B 16/mCD70-tumor bearing mice over a period of time (days) following administration of ⁇ )27-003 ⁇ CAR-transduced cells with (black bars) or without (horizontally striped bars) irradiation or cells transduced with a vector encoding GFP with (checkered bars) or without (unshaded bars) irradiation (500 Rads).
  • IFN serum interferon
  • Figure 3 is a graph showing IFN- ⁇ (pg/ml) secreted upon culture of human T cells transduced with an empty retroviral vector (control) (MSGV1 ) or one of ⁇ 27- ⁇ 3 ⁇ (SEQ ID NO: 7), ACD27-CD28 - ⁇ 3 ⁇ (SEQ ID NO: 8), ACD27-4-lBB - € ⁇ 3 ⁇ (SEQ ID NO: 9), ACD27-CD28 - 4-1 BB - ⁇ 3 ⁇ (SEQ ID NO: 10), fCD27-CD28 - ⁇ 3 ⁇ (SEQ ID NO: 1 1 ), fCD27-4-l BB - ⁇ 3 ⁇ (SEQ ID NO: 12), or fCD27-CD28 - 4-1 BB - ⁇ 3 ⁇ (SEQ ID NO: 13) alone (medium) (vertically striped bars) or upon co-culture with control target cells 624mel (checkered bars), 624/CD70 (black bars), 938mel (dotted bars), or
  • Figure 4 is a graph showing IFN- ⁇ (pg/ml) secreted upon culture of untransduced (UT) cells or retroviral packaging clone A2, A 10, B3, CI , E3, or G2 transduced with ACD27- 4-1 BB - CO3C, (SEQ ID NO: 9) alone (medium, vertically striped bars) or upon co-culture with control target cells SNU l 079 (dotted bars), SNU l 196 (white bars), 938mel (checkered bars), or 938/CD70 (black bars) or RCC target cells RCC 2245R (forward slashed bars), RCC 2246R (backslashed bars), RCC 2361 R (boxed bars), or RCC 1764 (herringbone bars).
  • Figure 5 is a graph showing IFN- ⁇ (pg/ml) secreted upon culture of untransduced (UT) cells or retroviral packaging clone A2, B l 1 , C5, or D2 transduced with ACD27-4-l BB - ⁇ 3 ⁇ (SEQ ID NO: 9) alone (medium, vertically striped bars) or upon co-culture with control target cells SNU l 079 (dotted bars), SNU l 196 (white bars), 938mel (checkered bars), or 938/CD70 (black bars) or RCC target cells RCC 2245R (forward slashed bars), RCC 2246R (backslashed bars), RCC 2361 R (boxed bars), or RCC 1764 (herringbone bars).
  • An embodiment of the invention provides a chimeric antigen receptor (CAR) having antigenic specificity for CD70, the CAR comprising: an antigen binding - transmembrane domain comprising a CD27 amino acid sequence lacking all or a portion of the CD27 intracellular T cell signaling domain, wherein the portion is at least amino acid residues 237 to 260 as defined by SEQ ID NO: 2; a 4-1 BB intracellular T cell signaling domain; a ⁇ 3 ⁇ intracellular T cell signaling domain; and optionally, a CD28 intracellular T cell signaling domain.
  • references to a "CAR" also refer to functional portions and functional variants of the CAR, unless specified otherwise.
  • a CAR is an artificially constructed hybrid protein or polypeptide containing the antigen binding domains of a receptor (e.g., a tumor necrosis factor (TNF) receptor) linked to T-cell signaling domains.
  • a receptor e.g., a tumor necrosis factor (TNF) receptor
  • Characteristics of CARs include their ability to redirect T-cell specificity and reactivity toward a selected target in a non-major histocompatibility complex (MHC)-restricted manner, exploiting the antigen-binding properties of receptors.
  • MHC histocompatibility complex
  • the non- MHC-restricted antigen recognition gives T cells expressing CARs the ability to recognize antigen independent of antigen processing, thus bypassing a major mechanism of tumor escape.
  • CARs advantageously do not dimerize with endogenous T cell receptor (TCR) alpha and beta chains.
  • phrases "have antigen(ic) specificity" and "elicit antigen-specific response,” as used herein, means that the CAR can specifically bind to and immunologically recognize an antigen, such that binding of the CAR to the antigen elicits an immune response.
  • CD70 belongs to the TNF superfamily and has the amino acid sequence of SEQ ID NO: 1
  • CD70 is a co- stimulatory molecule that is involved in the proliferation and survival of lymphoid-derived cells when it interacts with its receptor, CD27. Normal, non-cancerous expression of CD70 is restricted to lymphoid tissues such as activated T cells, B cells, natural killer (NK) cells, monocytes, and dendritic cells. CD70 is expressed in a variety of human cancers such as, for example, RCC (Diegmann et al., Eur. J.
  • the inventive CARs provide for one or more of any of the following: targeting and destroying CD70-expressing cancer cells, reducing or eliminating cancer cells, facilitating infiltration of immune cells to tumor site(s), and enhancing/extending anti-cancer responses. Because normal CD70 expression is limited to lymphoid tissues such as activated T cells, B cells, NK cells, monocytes, and dendritic cells, it is contemplated that the inventive CARs advantageously substantially avoid targeting/destroying many normal tissues.
  • An embodiment of the invention provides a CAR comprising an antigen binding - transmembrane domain comprising a CD27 amino acid sequence.
  • the CAR may comprise both a CD27 antigen binding domain and a CD27 transmembrane domain.
  • the CD27 may comprise or consist of any suitable human antigen binding - transmembrane domain CD27 amino acid sequence.
  • full-length CD27 including the antigen binding domain, the transmembrane domain, and the intracellular T cell signaling domain, has the amino acid sequence of SEQ ID NO: 2.
  • the antigen binding domain of CD27 is composed of amino acid residues 1-188 of SEQ ID NO: 2 and has the amino acid sequence of SEQ ID NO: 21
  • the transmembrane domain of CD27 is composed of amino acid residues 189-21 1 of SEQ ID NO: 2 and has the amino acid sequence of SEQ ID NO: 22
  • the intracellular T cell signaling domain of CD27 is composed of amino acid residues 212-260 of SEQ ID NO: 2 and has the amino acid sequence of SEQ ID NO: 23.
  • the CAR comprises an antigen binding - transmembrane domain comprising the amino acid sequences of SEQ ID NOs: 21 and 22.
  • the antigen binding domain of CD27 specifically binds to CD70.
  • An embodiment of the invention provides a CAR comprising an antigen binding - transmembrane domain comprising a CD27 amino acid sequence lacking all or a portion of the CD27 intracellular T cell signaling domain, wherein the portion that is lacking from the CAR is at least contiguous amino acid residues 237 to 260, at least contiguous amino acid residues 236 to 260, at least contiguous amino acid residues 235 to 260, at least contiguous amino acid residues 234 to 260, at least contiguous amino acid residues 233 to 260, at least contiguous amino acid residues 232 to 260, at least contiguous amino acid residues 231 to 260, at least contiguous amino acid residues 230 to 260, at least contiguous amino acid residues 229 to 260, at least contiguous amino acid residues 228 to 260, at least contiguous amino acid residues 227 to 260, at least contiguous amino acid residues 226 to 260, at least contiguous amino acid residues 237
  • the antigen binding - transmembrane domain comprises a CD27 amino acid sequence lacking contiguous amino acid residues 237 to 260, contiguous amino acid residues 236 to 260, contiguous amino acid residues 235 to 260, contiguous amino acid residues 234 to 260, contiguous amino acid residues 233 to 260, contiguous amino acid residues 232 to 260, contiguous amino acid residues 231 to 260, contiguous amino acid residues 230 to 260, contiguous amino acid residues 229 to 260, contiguous amino acid residues 228 to 260, contiguous amino acid residues 227 to 260, contiguous amino acid residues 226 to 260, contiguous amino acid residues 225 to 260, contiguous amino acid residues 224 to 260, contiguous amino acid residues 223 to 260, contiguous amino acid residues 222 to 260, contiguous amino acid residues 221 to 260, contiguous amino acid residues
  • the antigen binding - transmembrane domain comprises a CD27 amino acid sequence lacking all of the CD27 intracellular T cell signaling domain.
  • the antigen binding - transmembrane domain comprises a CD27 amino acid sequence lacking contiguous amino acid residues 212 to 260 as defined by SEQ ID NO: 2 or a CD27 amino acid sequence lacking contiguous amino acid residues 212 to 260 of SEQ ID NO: 2.
  • the antigen binding - transmembrane domain comprises a CD27 amino acid sequence lacking the amino acid sequence of SEQ ID NO: 23.
  • the antigen binding - transmembrane domain that comprises a CD27 amino acid sequence lacking all of the CD27 intracellular T cell signaling domain comprises or consists of an amino acid sequence at least about 90%, about 91 %, about 92%, about 93%, about 94%, about 95%, about 96%, about 97%, about 98%, or about 99% identical to SEQ ID NO: 3 or which comprises or consists of the amino acid sequence of SEQ ID NO: 3.
  • the CAR may further comprise a 4- I BB intracellular T cell signaling domain; a CD3 zeta ( ⁇ ) intracellular T cell signaling domain; and optionally, a CD28 intracellular T cell signaling domain.
  • the CAR comprises comprising a 4- 1 BB intracellular T cell signaling domain, a ⁇ 3 ⁇ intracellular T cell signaling domain, and a CD28 intracellular T cell signaling domain.
  • the CAR comprises a 4-1 BB intracellular T cell signaling domain and a ⁇ 3 ⁇ intracellular T cell signaling domain.
  • the 4-1 BB, ⁇ 3 ⁇ , and CD28 intracellular T cell signaling domains are human.
  • CD28 is a T cell marker important in T cell co- stimulation.
  • 4- I BB also known as CD 137, transmits a potent costimulatory signal to T cells, promoting differentiation and enhancing long-term survival of T lymphocytes.
  • ⁇ 3 ⁇ associates with TCRs to produce a signal and contains immunoreceptor tyrosine-based activation motifs (ITAMs).
  • ITAMs immunoreceptor tyrosine-based activation motifs
  • the ⁇ 3 ⁇ intracellular T cell signaling domain may comprise or consist of any suitable human ⁇ 3 ⁇ intracellular T cell signaling domain amino acid sequence.
  • the CO3C, intracellular T cell signaling domain comprises or consists of an amino acid sequence at least about 90%, about 91 %, about 92%, about 93%, about 94%, about 95%, about 96%, about 97%, about 98%, or about 99% identical to SEQ ID NO: 4.
  • the CO3C, intracellular T cell signaling domain comprises or consists of the amino acid sequence of SEQ ID NO: 4.
  • the 4-1 BB intracellular T cell signaling domain may comprise or consist of any suitable human 4-1 BB intracellular T cell signaling domain amino acid sequence.
  • the 4-1 BB intracellular T cell signaling domain comprises or consists of an amino acid sequence at least about 90%, about 91 %, about 92%, about 93%, about 94%,, about 95%, about 96%o, about 97%, about 98%o, or about 99% identical to SEQ ID NO: 5.
  • the 4- I BB intracellular T cell signaling domain comprises or consists of the amino acid sequence of SEQ ID NO: 5.
  • the CD28 intracellular T cell signaling domain may comprise or consist of any suitable human CD28 intracellular T cell signaling domain amino acid sequence.
  • the CD28 intracellular T cell signaling domain comprises or consists of an amino acid sequence at least about 90%, about 91 %, about 92%, about 93%, about 94%, about 95%, about 96%, about 97%, about 98%, or about 99% identical to SEQ ID NO: 6.
  • the CD28 intracellular T cell signaling domain comprises or consists of the amino acid sequence of SEQ ID NO: 6.
  • the CAR comprises a full-length CD27 amino acid sequence, including a CD27 antigen binding domain, a CD27 transmembrane domain, and a CD27 intracellular T cell signaling domain, in combination with a ⁇ 3 ⁇ intracellular T cell signaling domain (full length ( ⁇ ) ⁇ 27- ⁇ 3 ⁇ CAR).
  • the CAR may comprise or consist of a full-length CD27 amino acid sequence at least about 90%, about 91 %, about 92%, about 93%, about 94%, about 95%, about 96%, about 97%, about 98%, or about 99% identical to SEQ ID NO: 2 and any of the ⁇ 3 ⁇ amino acid sequences described herein with respect to other aspects of the invention.
  • the ⁇ 27- ⁇ 3 ⁇ CAR may comprise or consist of the full-length CD27 amino acid sequence of SEQ ID NO: 2 and the ⁇ 3 ⁇ amino acid sequence of SEQ ID NO: 4.
  • the ⁇ 27- ⁇ 3 ⁇ CAR may comprise or consist of an amino acid sequence at least about 90%, about 91 %, about 92%, about 93%, about 94%, about 95%, about 96%, about 97%, about 98%, or about 99% identical to SEQ ID NO: 7.
  • the fCD27-CD3C CAR comprises or consists of the amino acid sequence of SEQ ID NO: 7.
  • the ⁇ - ⁇ 3 ⁇ CAR lacks one or both of truncated CD 19 and DsRed.
  • the CAR comprises a full-length CD27 amino acid sequence, including a CD27 antigen binding domain, a CD27 transmembrane domain, and a CD27 intracellular T cell signaling domain, in combination with a ⁇ 3 ⁇ intracellular T cell signaling domain and a CD28 intracellular T cell signaling domain
  • the CAR may comprise or consist of any of the full- length CD27 amino acid sequences, any of the ⁇ 3 ⁇ amino acid sequences, and any of the CD28 amino acid sequences described herein with respect to other aspects of the invention.
  • the ⁇ 0 ⁇ 27-0 ⁇ 28-0 ⁇ 3 ⁇ CAR may comprise or consist of the full-length CD27 amino acid sequence of SEQ ID NO: 2, the CD3 ⁇ amino acid sequence of SEQ ID NO: 4, and the CD28 amino acid sequence of SEQ ID NO: 6.
  • the ⁇ 0027- ⁇ 28- ⁇ 3 ⁇ CAR may comprise or consist of an amino acid sequence at least about 90%, about 91 %, about 92%, about 93%, about 94%, about 95%, about 96%, about 97%, about 98%, or about 99% identical to SEQ ID NO: 1 1 .
  • the amino acid sequence at least about 90%, about 91 %, about 92%, about 93%, about 94%, about 95%, about 96%, about 97%, about 98%, or about 99% identical to SEQ ID NO: 1 1 .
  • the amino acid sequence at least about 90%, about 91 %, about 92%, about 93%, about 94%, about 95%, about 96%, about 97%, about 98%, or about 99% identical to SEQ ID NO: 1 1 .
  • the amino acid sequence at least about 90%, about 91 %, about 92%, about 93%, about 94%, about 95%, about 96%, about 97%, about 98%, or about 99% identical to SEQ ID NO: 1
  • fCD27-CD28-CI ⁇ CAR comprises or consists of the amino acid sequence of SEQ ID NO: 1 1 .
  • the CAR comprises a full-length CD27 amino acid sequence, including a CD27 antigen binding domain, a CD27 transmembrane domain, and a CD27 intracellular T cell signaling domain, in combination with a ⁇ 3 ⁇ intracellular T cell signaling domain and a 4- I BB intracellular T cell signaling domain
  • the CAR may comprise or consist of any of the full- length CD27 amino acid sequences, any of the ⁇ 3 ⁇ amino acid sequences, and any of the 4- 1BB amino acid sequences described herein with respect to other aspects of the invention.
  • the ⁇ 0 ⁇ 27-4-1 ⁇ -0 ⁇ 3 ⁇ CAR may comprise or consist of the full-length CD27 amino acid sequence of SEQ ID NO: 2, the CO3C, amino acid sequence of SEQ ID NO: 4, and the 4-1 BB amino acid sequence of SEQ ID NO: 5.
  • the ⁇ 27-4-1 ⁇ -003 ⁇ CAR may comprise or consist of an amino acid sequence at least about 90%), about 91 %, about 92%, about 93%, about 94%, about 95%, about 96%, about 97%, about 98%o, or about 99% identical to SEQ ID NO: 12.
  • the amino acid sequence at least about 90%
  • the amino acid sequence at least about 90%
  • the amino acid sequence at least about 9 %, about 92%, about 93%, about 94%, about 95%, about 96%, about 97%, about 98%o, or about 99% identical to SEQ ID NO: 12.
  • ⁇ 0027-4-1 ⁇ - ⁇ 3 ⁇ CAR comprises or consists of the amino acid sequence of SEQ ID NO: 12.
  • the CAR comprises a full-length CD27 amino acid sequence, including a CD27 antigen binding domain, a CD27 transmembrane domain, and a CD27 intracellular T cell signaling domain, in combination with a ⁇ 3 ⁇ intracellular T cell signaling domain, a 4- I BB intracellular T cell signaling domain, and a CD28
  • the CAR may comprise or consist of any of the full-length CD27 amino acid sequences, any of the 0 ⁇ 3 ⁇ amino acid sequences, any of the 4- I BB amino acid sequences, and any of the CD28 amino acid sequences described herein with respect to other aspects of the invention.
  • the ⁇ 0 ⁇ 27-0 ⁇ 28-4- 1 ⁇ -0 ⁇ 3 ⁇ CAR may comprise or consist of the full-length CD27 amino acid sequence of SEQ ID NO: 2, the ⁇ 3 ⁇ amino acid sequence of SEQ ID NO: 4, the 4- I BB amino acid sequence of SEQ ID NO: 5, and the CD28 amino acid sequence of SEQ ID NO: 6.
  • the ⁇ 0 ⁇ 27-0 ⁇ 28-4-1 ⁇ -0 ⁇ 3 ⁇ CAR may comprise or consist of an amino acid sequence at least about 90%, about 91 %, about 92%, about 93%, about 94%, about 95%, about 96%, about 97%, about 98%, or about 99% identical to SEQ ID NO: 1 3.
  • the fCD27-CD28-4-l BB-CD3C CAR comprises or consists of the amino acid sequence of SEQ ID NO: 13.
  • the CAR comprises a full-length mouse CD27 amino acid sequence, including a CD27 antigen binding domain, a CD27 transmembrane domain, and a CD27 intracellular T cell signaling domain, in combination with a mouse ⁇ 3 ⁇ intracellular T cell signaling domain ( ⁇ 0 ⁇ 27-0 ⁇ 3 ⁇ ).
  • the CAR may comprise or consist of a full-length mouse CD27 amino acid sequence at least about 90%, about 91 %, about 92%, about 93%, about 94%, about 95%, about 96%, about 97%, about 98%, or about 99% identical to SEQ ID NO: 26 in combination with a mouse CD3 ⁇ amino acid sequence at least about 90%, about 91 %, about 92%, about 93%, about 94%, about 95%, about 96%, about 97%, about 98%, or about 99% identical to SEQ ID NO: 27.
  • the ⁇ 2 ⁇ - ⁇ 3 ⁇ CAR may comprise or consist of the full-length mouse CD27 amino acid sequence of SEQ ID NO: 26 and the mouse ⁇ 3 ⁇ amino acid sequence of SEQ ID NO: 27.
  • the ⁇ 0 ⁇ 27-0 ⁇ 3 ⁇ CAR may comprise or consist of an amino acid sequence at least about 90%, about 91 %, about 92%, about 93%, about 94%, about 95%, about 96%, about 97%, about 98%, or about 99% identical to SEQ ID NO: 25.
  • the ⁇ 0 ⁇ 27-0 ⁇ 3 ⁇ CAR comprises or consists of the amino acid sequence of SEQ ID NO: 25.
  • the CAR comprises an antigen binding - transmembrane domain comprising a truncated CD27 amino acid sequence which lacks all of the CD27 intracellular T cell signaling domain, in combination with a ⁇ 3 ⁇ intracellular T cell signaling domain and a CD28 intracellular T cell signaling domain (truncated ( ⁇ ) CD27-CD28 - CO3Q.
  • the CAR may comprise or consist of a truncated CD27 antigen binding - transmembrane domain amino acid sequence at least about 90%, about 91 %, about 92%, about 93%, about 94%, about 95%, about 96%, about 97%, about 98%, or about 99% identical to SEQ ID NO: 3 in combination with any of the ⁇ 3 ⁇ intracellular T cell signaling domain amino acid sequences and any of the CD28 intracellular T cell signaling domain amino acid sequences described herein with respect to other aspects of the invention.
  • the ACD27-CD28 - ⁇ 3 ⁇ CAR may comprise or consist of the truncated CD27 antigen binding - transmembrane domain amino acid sequence of SEQ ID NO: 3, the CD3C amino acid sequence of SEQ ID NO: 4, and the CD28 amino acid sequence of SEQ ID NO: 6.
  • the ACD27-CD28 - CO3C, CAR may comprise or consist of an amino acid sequence at least about 90%, about 91 %, about 92%, about 93%, about 94%, about 95%, about 96%, about 97%, about 98%, or about 99% identical to SEQ ID NO: 8.
  • the ACD27-CD28 - ⁇ 3 ⁇ CAR comprises or consists of the amino acid sequence of SEQ ID NO: 8.
  • the CAR comprises an antigen binding - transmembrane domain comprising a truncated CD27 amino acid sequence which lacks all of the CD27 intracellular T cell signaling domain, in combination with a ⁇ 3 ⁇ intracellular T cell signaling domain and a 4- I BB intracellular T cell signaling domain (ACD27-4-lBB - ⁇ 3 ⁇ ).
  • the CAR may comprise or consist of any of the truncated CD27 antigen binding - transmembrane domain amino acid sequences, any of the ⁇ 3 ⁇ intracellular T cell signaling domain amino acid sequences, and any of the 4- I BB intracellular T cell signaling domain amino acid sequences described herein with respect to other aspects of the invention.
  • the ACD27-4-l BB - ⁇ 3 ⁇ CAR may comprise or consist of the truncated CD27 antigen binding - transmembrane domain amino acid sequence of SEQ ID NO: 3, the CO3C, amino acid sequence of SEQ ID NO: 4, and the 4- 1 BB amino acid sequence of SEQ ID NO: 5.
  • the ACD27-4-l BB - ⁇ 3 ⁇ CAR may comprise or consist of an amino acid sequence at least about 90%, about 91 %, about 92%, about 93%, about 94%, about 95%, about 96%, about 97%, about 98%, or about 99% identical to SEQ ID NO: 9.
  • the ACD27-4-l BB - ⁇ 3 ⁇ CAR comprises or consists of the amino acid sequence of SEQ ID NO: 9.
  • the CAR comprises an antigen binding - transmembrane domain comprising a truncated CD27 amino acid sequence which lacks all of the CD27 intracellular T cell signaling domain, in combination with a ⁇ 3 ⁇ intracellular T cell signaling domain, a CD28 intracellular T cell signaling domain, and a 4-1 BB
  • the CAR may comprise or consist of any of the truncated CD27 antigen binding - transmembrane domain amino acid sequences, any of the ⁇ 3 ⁇ intracellular T cell signaling domain amino acid sequences, any of the CD28 intracellular T cell signaling domain amino acid sequences, and any of the 4- I BB intracellular T cell signaling domain amino acid sequences described herein with respect to other aspects of the invention.
  • the ACD27-CD28 - 4- 1 BB - ⁇ 3 ⁇ CAR may comprise or consist of the truncated CD27 antigen binding - transmembrane domain amino acid sequence of SEQ ID NO: 3, the ⁇ 3 ⁇ amino acid sequence of SEQ ID NO: 4, the CD28 ammo acid sequence of SEQ ID NO: 6, and the 4-1 BB amino acid sequence of SEQ ID NO: 5.
  • the ACD27- CD28 - 4-1 BB - CD3 ⁇ CAR may comprise or consist of an amino acid sequence at least about 90%, about 91 %, about 92%, about 93%, about 94%, about 95%, about 96%, about 97%, about 98%, or about 99% identical to SEQ ID NO: 10.
  • the ACD27-CD28 - 4- I BB - ⁇ 3 ⁇ CAR comprises or consists of the amino acid sequence of SEQ ID NO: 10.
  • the CAR comprises an amino acid sequence at least about 90% identical to any one of SEQ ID NOs: 8-10. In an embodiment of the invention, the CAR comprises an amino acid sequence at least about 90% identical to SEQ ID NO: 9 or 10. In another embodiment of the invention, the CAR comprises an amino acid sequence at least about 90% identical to any one of SEQ ID NOs: 1 1 -13. In another embodiment of the invention, the CAR comprises an amino acid sequence at least about 90% identical to SEQ ID NO: 12 or 13. Preferably, the CAR comprises, consists of, or consists essentially of any one of the amino acid sequences set forth in Table 1 A. In a preferred embodiment of the invention, the CAR comprises the amino acid sequence of any one of SEQ ID NOs: 7-13. Preferably, the CAR comprises the amino acid sequence of any one of SEQ ID NO: 9, 10, 12, and 13.
  • the term "functional portion' ' when used in reference to a CAR refers to any part or fragment of the CAR of the invention, which part or fragment retains the biological activity of the CAR of which it is a part (the parent CAR).
  • Functional portions encompass, for example, those parts of a CAR that retain the ability to recognize target cells, or detect, treat, or prevent cancer, to a similar extent, the same extent, or to a higher extent, as the parent CAR.
  • the functional portion can comprise, for instance, about 10%, about 25%, about 30%, about 50%, about 68%, about 80%, about 90%, about 95%, or more, of the parent CAR.
  • the functional portion can comprise additional amino acids at the amino or carboxy terminus of the portion, or at both termini, which additional amino acids are not found in the amino acid sequence of the parent CAR.
  • the additional amino acids do not interfere with the biological function of the functional portion, e.g., recognize target cells, detect cancer, treat or prevent cancer, etc. More desirably, the additional amino acids enhance the biological activity, as compared to the biological activity of the parent CAR.
  • Functional variants include, for example, those variants of the CAR described herein (the parent CAR) that retain the ability to recognize target cells to a similar extent, the same extent, or to a higher extent, as the parent CAR.
  • the functional variant can, for instance, be at least about 30%, about 50%, about 75%, about 80%, about 90%, about 91 %, about 92%, about 93%, about 94%, about 95%, about 96%, about 97%, about 98%, about 99% or more identical in amino acid sequence to the parent CAR.
  • a functional variant can, for example, comprise the amino acid sequence of the parent CAR with at least one conservative amino acid substitution.
  • the functional variants can comprise the amino acid sequence of the parent CAR with at least one non-conservative amino acid substitution.
  • the non-conservative amino acid substitution may enhance the biological activity of the functional variant, such that the biological activity of the functional variant is increased as compared to the parent CAR.
  • Amino acid substitutions of the inventive CARs are preferably conservative amino acid substitutions.
  • Conservative amino acid substitutions are known in the art, and include amino acid substitutions in which one amino acid having certain physical and/or chemical properties is exchanged for another amino acid that has the same or similar chemical or physical properties.
  • the conservative amino acid substitution can be an acidic/negatively charged polar amino acid substituted for another acidic/negatively charged polar amino acid (e.g., Asp or Glu), an amino acid with a nonpolar side chain substituted for another amino acid with a nonpolar side chain (e.g., Ala, Gly, Val, He, Leu, Met, Phe, Pro, Trp, Cys, Val, etc.), a basic/positively charged polar amino acid substituted for another basic/positively charged polar amino acid (e.g.
  • an acidic/negatively charged polar amino acid substituted for another acidic/negatively charged polar amino acid e.g., Asp or Glu
  • an amino acid with a nonpolar side chain substituted for another amino acid with a nonpolar side chain e.g., Ala, Gly, Val, He, Leu, Met, Phe, Pro, Trp, Cys, Val, etc.
  • an uncharged amino acid with a polar side chain substituted for another uncharged amino acid with a polar side chain e.g., Asn, Gin, Ser, Thr, Tyr, etc.
  • an amino acid with a beta-branched side-chain substituted for another amino acid with a beta-branched side-chain e.g., He, Thr, and Val
  • an amino acid with an aromatic side-chain substituted for another amino acid with an aromatic side chain e.g., His, Phe, Tip, and Tyr
  • the CAR can consist essentially of the specified amino acid sequence or sequences described herein, such that other components, e.g., other amino acids, do not materially change the biological activity of the functional variant.
  • the CARs of embodiments of the invention can be of any length, i.e., can comprise any number of amino acids, provided that the CARs retain their biological activity, e.g., the ability to specifically bind to antigen, detect cancer cells in a mammal, or treat or prevent cancer in a mammal, etc.
  • the CAR can be about 50 to about 5000 amino acids long, such as 50, 70, 75, 100, 125, 150, 175, 200, 300, 400, 500, 600, 700, 800, 900, 1000 or more amino acids in length.
  • the CARs of embodiments of the invention can comprise synthetic amino acids in place of one or more naturally-occurring amino acids.
  • Such synthetic amino acids are known in the art, and include, for example, aminocyclohexane carboxylic acid, norleucine, a-amino n-decanoic acid, homoserine, S-acetylaminomethyl-cysteine, trans-3- and trans-4- hydroxyproline, 4-aminophenylalanine, 4- nitrophenylalanine, 4-chlorophenylalanine, 4- carboxyphenylalanine, ⁇ -phenylserine ⁇ -hydroxyphenylalanine, phenylglycine, - naphthylalanine, cyclohexylalanine, cyclohexylglycine, indoline-2-carboxylic acid, 1 ,2,3,4- tetrahydroisoquinoline-3-carboxylic acid, aminomalonic acid, aminomalonic acid,
  • the CARs of embodiments of the invention can be glycosylated, amidated, carboxylated, phosphorylated, esterified, N-acylated, cyclized via, e.g., a disulfide bridge, or converted into an acid addition salt and/or optionally dimerized or polymerized, or conjugated.
  • the CARs of embodiments of the invention can be obtained by methods known in the art such as, for example, de novo synthesis.
  • polypeptides and proteins can be recombinantly produced using the nucleic acids described herein using standard recombinant methods. See, for instance, Green and Sambrook, Molecular Cloning: A Laboratory Manual, 4 th ed., Cold Spring Harbor Press, Cold Spring Harbor, NY (2012).
  • the CARs described herein can be commercially synthesized by companies, such as Synpep (Dublin, CA), Peptide Technologies Corp. (Gaithersburg, MD), and Multiple Peptide Systems (San Diego, CA).
  • the inventive CARs can be synthetic, recombinant, isolated, and/or purified.
  • nucleic acid comprising a nucleotide sequence encoding any of the CARs described herein.
  • the nucleic acids of the invention may comprise a nucleotide sequence encoding any of the antigen binding domains, transmembrane domains, and/or intracellular T cell signaling domains described herein.
  • the nucleic acid comprises, consists of, or consists essentially of any one of the nucleotide sequences set forth in Table 1 B.
  • the nucleic acid comprises the nucleotide sequence of any one of SEQ ID NOs: 14-20.
  • the nucleic acid comprises the nucleotide sequence of any one of SEQ ID NOs: 16, 17, 19, and 20.
  • the nucleotide sequence encoding the fCD27-CD3 CAR does not encode one or both of truncated CD 19 and DsRed.
  • Nucleic acid as used herein includes “polynucleotide, “ 'Oligonucleotide,” and “nucleic acid molecule,” and generally means a polymer of D A or RNA, which can be single-stranded or double-stranded, synthesized or obtained (e.g., isolated and/or purified) from natural sources, which can contain natural, non-natural or altered nucleotides, and which can contain a natural, non-natural or altered internucleotide linkage, such as a phosphoroamidate linkage or a phosphorothioate linkage, instead of the phosphodiester found between the nucleotides of an unmodified oligonucleotide.
  • the nucleic acid does not comprise any insertions, deletions, inversions, and/or substitutions. However, it may be suitable in some instances, as discussed herein, for the nucleic acid to comprise one or more insertions, deletions, inversions, and/or substitutions. In some embodiments, the nucleic acid may encode additional amino acid sequences that do not affect the function of the CAR and which may or may not be translated upon expression of the nucleic acid by a host cell.
  • the nucleic acids of an embodiment of the invention may be recombinant.
  • the tenn "recombinant” refers to (i) molecules that are constructed outside living cells by joining natural or synthetic nucleic acid segments to nucleic acid molecules that can replicate in a living cell, or (ii) molecules that result from the replication of those described in (i) above.
  • the replication can be in vitro replication or in vivo replication.
  • a recombinant nucleic acid may be one that has a sequence that is not naturally occurring or has a sequence that is made by an artificial combination of two otherwise separated segments of sequence. This artificial combination is often accomplished by chemical synthesis or, more commonly, by the artificial manipulation of isolated segments of nucleic acids, e.g., by genetic engineering techniques, such as those described in Green and Sambrook, supra.
  • the nucleic acids can be constructed based on chemical synthesis and/or enzymatic ligation reactions using procedures known in the art. See, for example, Green and Sambrook, supra.
  • a nucleic acid can be chemically synthesized using naturally occurring nucleotides or variously modified nucleotides designed to increase the biological stability of the molecules or to increase the physical stability of the duplex formed upon hybridization (e.g., phosphorothioate derivatives and acridine substituted nucleotides).
  • modified nucleotides that can be used to generate the nucleic acids include, but are not limited to, 5-fluorouracil, 5-bromouracil, 5-chlorouracil, 5-iodouracil, hypoxanthine, xanthine, 4-acetylcytosine, 5-(carboxyhydroxymethyl) uracil, 5-carboxymethylaminomethyl- 2-thiouridine, 5-carboxymethylaminomethyluracil, dihydrouracil, beta-D-galactosylqueosine, inosine, N 6 -isopentenyladenine, 1 -methyl guanine, 1 -methylinosine, 2,2-dimethylguanine, 2- methyladenine, 2-methylguanine, 3-methylcytosine, 5-methylcytosine, N 6 -substituted adenine, 7-methylguanine, 5-methylaminomethyluracil, 5-methoxyaminomethyl-2-thiouracil, beta-D
  • nucleic acids of the invention can be purchased from companies, such as Macromolecular Resources (Fort Collins, CO) and Synthegen (Houston, TX).
  • the nucleic acid can comprise any isolated or purified nucleotide sequence which encodes any of the CARs described herein with respect to other aspects of the invention.
  • nucleotide sequence can comprise a nucleotide sequence which is degenerate to any of the sequences or a combination of degenerate sequences.
  • An embodiment of the invention also provides an isolated or purified nucleic acid comprising a nucleotide sequence which is complementary to the nucleotide sequence of any of the nucleic acids described herein or a nucleotide sequence which hybridizes under stringent conditions to the nucleotide sequence of any of the nucleic acids described herein.
  • the nucleotide sequence which hybridizes under stringent conditions may hybridize under high stringency conditions.
  • high stringency conditions is meant that the nucleotide sequence specifically hybridizes to a target sequence (the nucleotide sequence of any of the nucleic acids described herein) in an amount that is detectably stronger than non-specific hybridization.
  • High stringency conditions include conditions which would distinguish a polynucleotide with an exact complementary sequence, or one containing only a few scattered mismatches from a random sequence that happened to have a few small regions (e.g., 3-10 bases) that matched the nucleotide sequence. Such small regions of
  • Relatively high stringency conditions would include, for example, low salt and/or high temperature conditions, such as provided by about 0.02-0.1 M NaCl or the equivalent, at temperatures of about 50-70 °C. Such high stringency conditions tolerate little, if any, mismatch between the nucleotide sequence and the template or target strand, and are particularly suitable for detecting expression of any of the inventive CARs. It is generally appreciated that conditions can be rendered more stringent by the addition of increasing amounts of formamide.
  • the invention also provides a nucleic acid comprising a nucleotide sequence that is at least about 70% or more, e.g., about 80%, about 90%, about 91 %, about 92%, about 93%, about 94%, about 95%, about 96%, about 97%, about 98%, or about 99% identical to any of the nucleic acids described herein.
  • the nucleic acids of the invention can be incorporated into a recombinant expression vector.
  • an embodiment of the invention provides recombinant expression vectors comprising any of the nucleic acids of the invention.
  • the term "recombinant expression vector” means a genetically-modified oligonucleotide or polynucleotide construct that permits the expression of an mRNA, protein, polypeptide, or peptide by a host cell, when the construct comprises a nucleotide sequence encoding the mRNA, protein, polypeptide, or peptide, and the vector is contacted with the cell under conditions sufficient to have the mRNA, protein, polypeptide, or peptide expressed within the cell.
  • the vectors of the invention are not naturally-occurring as a whole.
  • the inventive recombinant expression vectors can comprise any type of nucleotides, including, but not limited to DNA and RNA, which can be single-stranded or double-stranded, synthesized or obtained in part from natural sources, and which can contain natural, non-natural or altered nucleotides.
  • the recombinant expression vectors can comprise naturally-occurring or non-naturally-occurring intemucleotide linkages, or both types of linkages.
  • the non-naturally occurring or altered nucleotides or intemucleotide linkages do not hinder the transcription or replication of the vector.
  • the recombinant expression vector comprising the nucleotide sequence encoding the ⁇ 0 ⁇ 27-0 ⁇ 3 ⁇ CAR does not encode one or both of truncated CD 19 and DsRed.
  • the recombinant expression vector of the invention can be any suitable recombinant expression vector, and can be used to transform or transfect any suitable host cell.
  • Suitable vectors include those designed for propagation and expansion or for expression or both, such as plasmids and viruses.
  • the vector can be selected from the group consisting of the pUC series (Fermentas Life Sciences, Glen Burnie, MD), the pBluescript series (Stratagene, LaJolla, CA), the pET series (Novagen, Madison, WI), the pGEX series (Pharmacia Biotech, Uppsala, Sweden), and the pEX series (Clontech, Palo Alto, CA).
  • Bacteriophage vectors such as ⁇ ⁇ , ⁇ ' ⁇ 1 , ZapII (Stratagene), XEMBL4, and ⁇ 149, also can be used.
  • plant expression vectors include pBIOl , pBI101.2, pBI101.3, pBI121 and pBIN19 (Clontech).
  • animal expression vectors include pEUK-Cl, pMAM, and pMAMneo (Clontech).
  • the recombinant expression vector may be a viral vector, e.g., a retroviral vector or a lentiviral vector. In some embodiments, the vector can be a transposon.
  • the recombinant expression vectors of the invention can be prepared using standard recombinant DNA techniques described in, for example, Green and Sambrook, supra.
  • Constructs of expression vectors, which are circular or linear, can be prepared to contain a replication system functional in a prokaryotic or eukaryotic host cell.
  • Replication systems can be derived, e.g., from ColEl, 2 ⁇ plasmid, ⁇ , SV40, bovine papilloma virus, and the like.
  • the recombinant expression vector may comprise regulatory sequences, such as transcription and translation initiation and termination codons, which are specific to the type of host cell (e.g., bacterium, fungus, plant, or animal) into which the vector is to be introduced, as appropriate, and taking into consideration whether the vector is DNA- or RNA-based.
  • the recombinant expression vector may comprise restriction sites to facilitate cloning.
  • the recombinant expression vector can include one or more marker genes, which allow for selection of transformed or transfected host cells.
  • Marker genes include biocide resistance, e.g., resistance to antibiotics, heavy metals, etc., complementation in an auxotrophic host to provide prototrophy, and the like.
  • Suitable marker genes for the inventive expression vectors include, for instance, neomycin/G418 resistance genes, hygromycin resistance genes, histidinol resistance genes, tetracycline resistance genes, and ampicillin resistance genes.
  • the recombinant expression vector can comprise a native or nonnative promoter operably linked to the nucleotide sequence encoding the CAR, or to the nucleotide sequence which is complementary to or which hybridizes to the nucleotide sequence encoding the CAR.
  • the selection of promoters e.g., strong, weak, inducible, tissue-specific and developmental-specific, is within the ordinary skill of the artisan.
  • the combining of a nucleotide sequence with a promoter is also within the skill of the artisan.
  • the promoter can be a non-viral promoter or a viral promoter, e.g., a cytomegalovirus (CMV) promoter, an SV40 promoter, an RSV promoter, or a promoter found in the long-terminal repeat of the murine stem cell virus.
  • CMV cytomegalovirus
  • inventive recombinant expression vectors can be designed for either transient expression, for stable expression, or for both. Also, the recombinant expression vectors can be made for constitutive expression or for inducible expression.
  • the recombinant expression vectors can be made to include a suicide gene.
  • suicide gene refers to a gene that causes the cell expressing the suicide gene to die.
  • the suicide gene can be a gene that confers sensitivity to an agent, e.g., a drug, upon the cell in which the gene is expressed, and causes the cell to die when the cell is contacted with or exposed to the agent.
  • Suicide genes are known in the art and include, for example, the Herpes Simplex Vims (HSV) thymidine kinase (TK) gene, cytosine daminase, purine nucleoside phosphorylase, and nitroreductase.
  • An embodiment of the invention further provides a host cell comprising any of the recombinant expression vectors described herein.
  • the term "host cell'" refers to any type of cell that can contain the inventive recombinant expression vector.
  • the host cell can be a eukaryotic cell, e.g., plant, animal, fungi, or algae, or can be a prokaryotic cell, e.g., bacteria or protozoa.
  • the host cell can be a cultured cell or a primary cell, i.e., isolated directly from an organism, e.g., a human.
  • the host cell can be an adherent cell or a suspended cell, i.e., a cell that grows in suspension.
  • Suitable host cells are known in the art and include, for instance, DH5a E. coli cells, Chinese hamster ovarian cells, monkey VERO cells, COS cells, HEK293 cells, and the like.
  • the host cell may be a prokaryotic cell, e.g., a DH5a cell.
  • the host cell may be a mammalian cell.
  • the host cell may be a human cell.
  • the host cell can be of any cell type, can originate from any type of tissue, and can be of any developmental stage, the host cell may be a peripheral blood lymphocyte (PBL) or a peripheral blood mononuclear cell (PBMC).
  • PBL peripheral blood lymphocyte
  • PBMC peripheral blood mononuclear cell
  • the host cell may be a T cell.
  • the T cell can be any T cell, such as a cultured T cell, e.g., a primary T cell, or a T cell from a cultured T cell line, e.g., Jurkat, SupTl , etc., or a T cell obtained from a mammal. If obtained from a mammal, the T cell can be obtained from numerous sources, including but not limited to blood, bone marrow, lymph node, the thymus, or other tissues or fluids. T cells can also be enriched for or purified.
  • the T cell may be a human T cell.
  • the T cell may be a T cell isolated from a human.
  • the T cell can be any type of T cell and can be of any developmental stage, including but not limi ted to, CD4 CD8 double positive T cells, CD4 + helper T cells, e.g., Thi and Th 2 cells, CD8 ' T cells (e.g., cytotoxic T cells), tumor infiltrating cells, memory T cells, naive T cells, and the like.
  • the T cell may be a CD8 + T cell or a CD4 + T cell.
  • a population of cells comprising at least one host cell described herein.
  • the population of cells can be a heterogeneous population comprising the host cell comprising any of the recombinant expression vectors described, in addition to at least one other cell, e.g., a host cell (e.g., a T cell), which does not comprise any of the recombinant expression vectors, or a cell other than a T cell, e.g., a B cell, a macrophage, a neutrophil, an erythrocyte, a hepatocyte, an endothelial cell, an epithelial cell, a muscle cell, a brain cell, etc.
  • a host cell e.g., a T cell
  • a cell other than a T cell e.g., a B cell, a macrophage, a neutrophil, an erythrocyte, a hepatocyte, an endothelial cell, an epithelial cell, a muscle cell,
  • the population of cells can be a substantially homogeneous population, in which the population comprises mainly host cells (e.g., consisting essentially of) comprising the recombinant expression vector.
  • the population also can be a clonal population of cells, in which all cells of the population are clones of a single host cell comprising a recombinant expression vector, such that all cells of the population comprise the recombinant expression vector.
  • the population of cells is a clonal population comprising host cells comprising a recombinant expression vector as described herein.
  • the numbers of cells in the population may be rapidly expanded. Expansion of the numbers of cells expressing the CAR can be
  • expansion of the numbers of cells is carried out by culturing the T cells with OKT3 antibody, IL-2, and feeder PBMC (e.g., irradiated allogeneic PBMC).
  • OKT3 antibody IL-2
  • feeder PBMC e.g., irradiated allogeneic PBMC
  • CARs, nucleic acids, recombinant expression vectors, and host cells can be isolated and/or purified.
  • isolated means having been removed from its natural environment.
  • a purified (or isolated) host cell preparation is one in which the host cell is more pure than cells in their natural environment within the body. Such host cells may be produced, for example, by standard purification techniques.
  • a preparation of a host cell is purified such that the host cell represents at least about 50%, for example at least about 70%, of the total cell content of the preparation.
  • the purity can be at least about 50%, can be greater than about 60%, about 70% or about 80%, or can be about 100%.
  • inventive CAR materials can be formulated into a composition, such as a pharmaceutical composition.
  • a pharmaceutical composition comprising any of the CARs, nucleic acids, expression vectors, and host cells (including populations thereof), and a pharmaceutically acceptable carrier.
  • inventive pharmaceutical compositions containing any of the inventive CAR materials can comprise more than one inventive CAR material, e.g., a CAR and a nucleic acid, or two or more different CARs.
  • the pharmaceutical composition can comprise an inventive CAR material in combination with other pharmaceutically active agents or drugs, such as chemotherapeutic agents, e.g., asparaginase, busulfan, carboplatin, cisplatin, daunorubicin, doxorubicin, iluorouracil, gemcitabine, hydroxyurea, methotrexate, paclitaxel, rituximab, vinblastine, vincristine, etc.
  • the pharmaceutical composition comprises the inventive host cell or populations thereof.
  • the carrier is a pharmaceutically acceptable carrier.
  • the carrier can be any of those conventionally used for the particular inventive CAR material under consideration.
  • Such pharmaceutically acceptable carriers are well-known to those skilled in the art and are readily available to the public. It is preferred that the pharmaceutically acceptable carrier be one which has no detrimental side effects or toxicity under the conditions of use.
  • Suitable formulations may include any of those for oral, parenteral, subcutaneous, intravenous, intramuscular, intraarterial, intrathecal, or interperitoneal administration. More than one route can be used to administer the inventive CAR materials, and in certain instances, a particular route can provide a more immediate and more effective response than another route.
  • the inventive CAR material is administered by injection, e.g., intravenously.
  • the pharmaceutically acceptable earner for the cells for injection may include any isotonic earner such as, for example, normal saline (about 0.90% w/v of NaCl in water, about 300 mOsm/L NaCl in water, or about 9.0 g NaCl per liter of water), NORMOSOL R electrolyte solution (Abbott, Chicago, IL), PLASMA-LYTE A (Baxter, Deerfield, IL), about 5% dextrose in water, or Ringer's lactate.
  • the pharmaceutically acceptable earner is supplemented with human serum albumen.
  • the dose of the inventive C AR material also will be determined by the existence, nature and extent of any adverse side effects that might accompany the administration of a particular inventive CAR material. Typically, the attending physician will decide the dosage of the inventive CAR material with which to treat each individual patient, taking into consideration a variety of factors, such as age, body weight, general health, diet, sex, inventive CAR material to be administered, route of administration, and the severity of the cancer being treated.
  • the inventive CAR material is a population of cells
  • the number of cells administered per infusion may vary, e.g., from about 1 x 10 6 to about 1 x 1 0 12 cells or more. In certain embodiments, fewer than 1 x 10 6 cells may be administered.
  • the amount or dose of the inventive CAR material administered should be sufficient to effect a therapeutic or prophylactic response in the subject or animal over a reasonable time frame.
  • the dose of the inventive CAR material should be sufficient to bind to antigen, or detect, treat or prevent cancer in a period of from about 2 hours or longer, e.g., about 12 to about 24 or more hours, from the time of administration. In certain embodiments, the time period could be even longer.
  • the dose will be determined by the efficacy of the particular inventive CAR material and the condition of the animal (e.g., human), as well as the body weight of the animal (e.g., human) to be treated.
  • an assay which comprises, for example, comparing the extent to which target cells are lysed and/or IFN- ⁇ is secreted by T cells expressing the inventive CAR upon administration of a given dose of such T cells to a mammal, among a set of mammals of which is each given a different dose of the T cells, could be used to determine a starting dose to be administered to a mammal.
  • the extent to which target cells are lysed and/or IFN- ⁇ is secreted upon administration of a certain dose can be assayed by methods known in the art.
  • inventive CAR materials of the invention can be modified in any number of ways, such that the therapeutic or prophylactic efficacy of the inventive CAR materials is increased through the
  • inventive CAR materials can be conjugated either directly or indirectly through a linker to a targeting moiety.
  • the practice of conjugating compounds, e.g., inventive CAR materials, to targeting moieties is known in the art.
  • one or more additional therapeutic agents can be coadministered to the mammal.
  • coadministering is meant administering one or more additional therapeutic agents and the inventive CAR materials sufficiently close in time such that the inventive CAR materials can enhance the effect of one or more additional therapeutic agents, or vice versa.
  • the inventive CAR materials can be administered first and the one or more additional therapeutic agents can be administered second, or vice versa.
  • the inventive CAR materials and the one or more additional therapeutic agents can be administered simultaneously.
  • An exemplary therapeutic agent that can be co-administered with the CAR materials is IL-2. It is believed that IL-2 enhances the therapeutic effect of the inventive CAR materials.
  • inventive pharmaceutical compositions, CARs, nucleic acids, recombinant expression vectors, host cells, or populations of cells can be used in methods of treating or preventing cancer in a mammal.
  • inventive CARs have biological activity, e.g., ability to recognize antigen, e.g., CD70, such that the CAR when expressed by a cell is able to mediate an immune response against the cell expressing the antigen, e.g., CD70, for which the CAR is specific.
  • an embodiment of the invention provides a method of treating or preventing cancer in a mammal, comprising administering to the mammal the CARs, the nucleic acids, the recombinant expression vectors, the host cells, the population of cells, and/or the pharmaceutical compositions of the invention in an amount effective to treat or prevent cancer in the mammal.
  • An embodiment of the invention further comprises lymphodepleting the mammal prior to administering the inventive CAR materials.
  • lymphodepletion include, but may not be limited to, nonmyeloablative lymphodepleting chemotherapy, myeloablative lymphodepleting chemotherapy, total body irradiation, etc.
  • the cells can be cells that are allogeneic or autologous to the mammal.
  • the cells are autologous to the mammal.
  • the mammal referred to herein can be any mammal.
  • the term "mammal” refers to any mammal, including, but not limited to, mammals of the order Rodentia, such as mice and hamsters, and mammals of the order Logomorpha, such as rabbits.
  • the mammals may be from the order Carnivora, including Felines (cats) and Canines (dogs).
  • the mammals may be from the order Artiodactyla, including Bovines (cows) and Swines (pigs) or of the order Perssodactyla, including Equines (horses).
  • the mammals may be of the order Primates, Ceboids, or Simoids (monkeys) or of the order Anthropoids (humans and apes).
  • the mammal is a human.
  • the cancer can be any cancer, including any of acute lymphocytic cancer, acute myeloid leukemia, alveolar rhabdomyosarcoma, bladder cancer (e.g., bladder carcinoma), bone cancer, brain cancer (e.g., medulloblastoma), breast cancer, cancer of the anus, anal canal, or anorectum, cancer of the eye, cancer of the intrahepatic bile duct, cancer of the joints, cancer of the neck, gallbladder, or pleura, cancer of the nose, nasal cavity, or middle ear, cancer of the oral cavity, cancer of the vulva, chronic lymphocytic leukemia (CLL), chronic myeloid cancer, colon cancer, esophageal cancer, cervical cancer, fibrosarcoma, gastrointestinal carcinoid tumor, head and neck cancer (e.g., head and neck squamous cell carcinoma), glioblastoma, Hodgkin's lymphoma, hypopha
  • the cancer is characterized by the expression of CD70.
  • the cancer is any of RCC (for example, ccRCC), glioblastoma, NHL, CLL, diffuse large-B-cell lymphoma, and follicular lymphoma.
  • inventive methods can provide any amount of any level of treatment or prevention of cancer in a mammal.
  • the treatment or prevention provided by the inventive method can include treatment or prevention of one or more conditions or symptoms of the disease, e.g., cancer, being treated or prevented.
  • prevention can encompass delaying the onset of the disease, or a symptom or condition thereof.
  • Another embodiment of the invention provides a use of the inventive CARs, nucleic acids, recombinant expression vectors, host cells, populations of cells, or
  • compositions for the treatment or prevention of cancer in a mammal.
  • Another embodiment of the invention provides a method of detecting the presence of cancer in a mammal, comprising: (a) contacting a sample comprising one or more cells from the mammal with the CARs, the nucleic acids, the recombinant expression vectors, the host cells, or the population of cells, of the invention, thereby forming a complex, (b) and detecting the complex, wherein detection of the complex is indicative of the presence of cancer in the mammal.
  • the sample may be obtained by any suitable method, e.g., biopsy or necropsy.
  • a biopsy is the removal of tissue and/or cells from an individual. Such removal may be to collect tissue and/or cells from the individual in order to perform experimentation on the removed tissue and/or cells. This experimentation may include experiments to determine if the individual has and/or is suffering from a certain condition or disease-state.
  • the condition or disease may be, e.g., cancer.
  • the sample comprising cells of the mammal can be a sample comprising whole cells, lysates thereof, or a fraction of the whole cell lysates, e.g., a nuclear or cytoplasmic fraction, a whole protein fraction, or a nucleic acid fraction.
  • the cells can be any cells of the mammal, e.g., the cells of any organ or tissue, including blood cells or endothelial cells.
  • the contacting can take place in vitro or in vivo with respect to the mammal.
  • the contacting is in vitro.
  • detection of the complex can occur through any number of ways known in the art.
  • the inventive CARs, polypeptides, proteins, nucleic acids, recombinant expression vectors, host cells, or populations of cells, described herein can be labeled with a detectable label such as, for instance, a radioisotope, a fluorophore (e.g., fluorescein isothiocyanate (FITC), phycoerythrin (PE)), an enzyme (e.g., alkaline phosphatase, horseradish peroxidase), and element particles (e.g., gold particles).
  • a detectable label such as, for instance, a radioisotope, a fluorophore (e.g., fluorescein isothiocyanate (FITC), phycoerythrin (PE)), an enzyme (e.g., alkaline phosphatase, horseradish peroxidase), and element particles (e.g., gold particles).
  • CAR function can be evaluated by measurement of cellular cytoxicity, as described in Zhao et al., J. Immunol., 174: 4415-4423 (2005).
  • This example demonstrates the transduction efficiency of a retroviral vector encoding a CAR including full-length mouse CD27 and a mouse CD3 ⁇ T cell intracellular signaling domain ( ⁇ 0 ⁇ 27-0 ⁇ 3 ⁇ CAR) and having the amino acid sequence of SEQ ID NO: 25 and the reactivity of the ⁇ 27-0 ⁇ 3 ⁇ CAR against mCD70-expressing tumor cells in vitro.
  • a retroviral vector encoding a CAR including full-length mouse CD27 and a mouse CD3 ⁇ T cell intracellular signaling domain ( ⁇ 0 ⁇ 27-0 ⁇ 3 ⁇ CAR) and having the amino acid sequence of SEQ ID NO: 25 was constructed.
  • Murine T cells were retrovirally transduced with the ⁇ " ⁇ 27- ⁇ 3 ⁇ CAR retroviral vector. Transduction efficiency was determined to be 62.6%.
  • Mouse T cells generated from splenocytes were untransduced (UT) or transduced with a vector encoding GFP or the mCDll- D ⁇ CAR (effector cells) and cultured alone (medium) or co-cultured with B16 melanoma cells that do not express mouse CD70 (B16 cells) or B16 cells that were transduced to express mouse CD70 (B 16/mCD70) target cells.
  • Pmel cells which are mouse T cells that recognize Bl 6 tumor, were used as a positive control effector cell. IFN- ⁇ secretion was measured. The results are shown in Table 2. As shown in Table 2, cells transduced with the ⁇ 0 ⁇ 27-0 ⁇ 3 ⁇ CAR showed high reactivity against CD70- expressing tumors in vitro.
  • mice generated from splenocytes transduced with a nucleotide sequence encoding a CAR including full-length mouse CD27 and a mouse ⁇ 3 ⁇ T cell intracellular signaling domain ( ⁇ 0 ⁇ ) 27-0 ⁇ 3 ⁇ CAR) and having the amino acid sequence of SEQ ID NO: 25 reduces tumor burden and increases the survival of CD70-expressing tumor-bearing mice.
  • mice were established in mice by injecting them with B 16 cells or B16/mCD70 cells.
  • splenocytes were removed from the mice and stimulated with concanavalin A (ConA) and IL-7 or anti-mouse CD3 (mCD3) and soluble CD28 (sCD28).
  • ConA concanavalin A
  • mCD3 anti-mouse CD3
  • sCD28 soluble CD28
  • the ⁇ 0 ⁇ 27-0 ⁇ 3 ⁇ CAR-transduced cells (1 x 10 7 ) were administered to the tumor- bearing mice, and the mice were irradiated (500 rads).
  • Control tumor-bearing mice were administered untransduced cells, phosphate buffered saline (PBS), or a combination of pmel cells (pmel), a gp l OO vaccine (V), and IL-2 (I) ("pmel + VI”)and irradiated.
  • PBS phosphate buffered saline
  • pmel gp l OO vaccine
  • I IL-2
  • mice bearing CD70+ tumors could be successfully treated with ⁇ 0 ⁇ 27-0 ⁇ 3 ⁇ CAR-transduced cells, and the treatment was CD70-specific.
  • B16/mCD70 tumor-bearing mice were administered mCD27-CD3C CAR-transduced cells at a dose of 1 x 10 4 , 1 x 10 5 , 1 x 10 6 , or 1 x 10 7 cells per mouse with or without irradiation (500 Rads).
  • Control tumor- bearing mice were administered PBS, pmel + VI, or mouse T cells that were transduced with an empty vector with or without irradiation (500 Rads). The results are shown in Figures 1C- 1 D.
  • B16 or B16/mCD70-tumor bearing mice were administered untransduced cells or cells transduced with the ⁇ 0 ⁇ 27-0 ⁇ 3 ⁇ CAR having the amino acid sequence of SEQ ID NO: 25, PBS, or pmel + V, with or without irradiation (500 Rads).
  • the average weight of the mice was measured over a period beginning about six days after cell transfer up to about 17 days following treatment.
  • the results are shown in Figures 2A-2D.
  • transient lower body weights were observed for both B16/mCD70 and B16-tumor bearing mice that were treated with the ⁇ 27-003 ⁇ CAR.
  • the lower body weight observed in the ⁇ 27 ⁇ 3 ⁇ CAR-treated mice was irrelevant to implanted tumors.
  • mice recovered lost body weight when they were administered a hydro gel containing water, hydrocolloids, food acid, and sodium benzoate.
  • B 16 or B 16/mCD70-tumor bearing mice were administered untransduced cells or cells transduced with the ⁇ 0 ⁇ 27-0 ⁇ 3 ⁇ CAR having the amino acid sequence of SEQ ID NO: 25, or cells transduced with a vector encoding GFP, with or without irradiation (500 Rads).
  • the absolute white blood cell (WBC) count in the mice was measured over a period beginning about six days after cell transfer up to about 14 days following treatment.
  • the results are shown in Figures 2E-2H.
  • a transient lower WBC count was observed in the mice that were treated with the mCD27-CO3 ⁇ CAR.
  • a transient lower splenocyte count was also observed in the mice that were treated with the mCD27-CD3C CAR.
  • Bl 6/mCD70-tumor bearing mice were administered cells transduced with the ⁇ 027-0 ⁇ 3 ⁇ CAR having the amino acid sequence of SEQ ID NO: 25 or cells transduced with a vector encoding GFP, with or without irradiation (500 Rads). Serum IFN- ⁇ levels were measured for a period beginning about three days after cell transfer up to about seven days after treatment. The results are shown in Figure 21. As shown in Figure 21, transient IFN- ⁇ secretion was observed in the irradiated mice treated with the ⁇ 0 ⁇ 27-0 ⁇ 3 ⁇ CAR.
  • Non-tumor bearing mice were administered cells that were transduced with the ⁇ 27- ⁇ 3 ⁇ CAR having the amino acid sequence of SEQ ID NO: 25 or cells transduced with a vector encoding GFP (GFP), with or without irradiation (500 Rads).
  • the mice were immunized with ovalbumin (OVA) or human (h) gpl OO 32 or 50 days after transfer of transduced cells.
  • OVA ovalbumin
  • h human gpl OO 32 or 50 days after transfer of transduced cells.
  • T cells were removed from the spleen and lymph node (LN) of the mice seven days after immunization. The cells were stimulated in vitro with OT-1 , OT-II, or hgpl OO peptide.
  • mice The results are shown in Table 3 (Day 32 - spleen), Table 4 (Day 32 - LN), and Table 5 (Day 50 - spleen).
  • Table 5 immunized C57BL/6 (immune competent) mice (B6/Im) were used as a positive control.
  • Na ' ive C57BL/6 mice (B6/naive) were used as a negative control.
  • Tables 3-5 administration of the ⁇ " ⁇ 0027- ⁇ 3 ⁇ CAR does not have a measurable effect on the long-term immune function of non-tumor bearing mice.
  • the histology of various organs including brain, lung, liver, kidney, intestine, heart, spleen, and bone were examined from 3 days to 7 days after cell transfer.
  • the chemistry of the blood in particular, the blood levels of sodium, potassium, chloride, calcium, magnesium, phosphorus, glucose, blood urea nitrogen (BUN), creatinine, uric acid, albumin, protein, cholesterol, triglycerides, alkaline phosphatase (ALK P),
  • ALT/GPT alanineaminotransferase
  • AST/GOT aspartate aminotransferase
  • amylase amylase
  • CK creatine kinase
  • LD lactate dehydrogenase
  • T cells transduced with a nucleotide sequence encoding a CAR including full-length human CD27 and a human CD3 ⁇ T cell intracellular signaling domain express the CAR following expansion of the numbers of transduced cells.
  • PBL were non-specifically stimulated with OKT3 and T cells generated from the PBL were (a) untransduced (UT), (b) transduced with a nucleotide sequence encoding full- length human CD27 (fCD27), or (c) transduced with a nucleotide sequence encoding the fCD27-CD3C, CAR having the amino acid sequence of SEQ ID NO: 7.
  • the cells were grown, analyzed for CAR expression by fluorescence-activated cell sorting (FACS), and tested for tumor reactivity based on IFN- ⁇ production.
  • the numbers of CD70-reactive cells were rapidly expanded (REP) generally as described in Riddell et al., J. Immunol.
  • T cells transduced with a nucleotide sequence encoding a CAR including full-length human CD27 and a human CD3 ⁇ T cell intracellular signaling domain (fCO2T-CO3 > CAR) proliferate upon co-culture with CD70-expressing cells and specifically recognize CD70-expressing tumor cell lines in vitro.
  • T cells were generated from human PBL. Untransduced (UT) T cells or T cells transduced with a nucleotide sequence encoding fCD27 or the ⁇ 0 ⁇ 27-0 ⁇ 3 ⁇ CAR (effector cells) were cultured alone or co-cultured with CD70-expressing tumor cell line 624mel or 624mel cells transduced with CD70 (624/CD70) (target cells). Proliferation of the effector cells was measured using carboxyfluorescein succinimidyl ester (CFSE) on day 4 of the co- culture. The T cells transduced with the ⁇ 27-003 ⁇ CAR proliferated only when co- cultured with the CD70-expressing tumor cell line 624/CD70. The UT T cells and the T cells transduced with fCD27 did not proliferate in any culture.
  • CFSE carboxyfluorescein succinimidyl ester
  • UT T cells or T cells transduced with a nucleotide sequence encoding fCD27 or the fCD27-CD3C CAR (SEQ ID NO: 7) (effector cells) were cultured alone (medium) or co- cultured with one of the human RCC cell lines or control cell lines 624, 624/CD70, SNU245, SNU 1 079, or SNU 1 196 (target cells) shown in Table 8 below. All SNU cell lines were CD70 negative. IFN- ⁇ secretion was measured. The results are shown in Table 8. As shown in Table 8, T cells transduced with a nucleotide sequence the ⁇ 27- ⁇ 3 ⁇ CAR (SEQ ID NO: 7) were reactive against CD70-expressing human RCC cell lines.
  • CARs including a truncated ( ⁇ ) CD27 lack all of the CD27 intracellular T cell signaling domain, that is, the truncated CD27 lacks contiguous amino acid residues 212-260 of SEQ ID NO: 2.
  • Transduced cells were analyzed for CD3, CD27, CD62L, and CD45RO expression by FACS.
  • Tables 9A-9C show the percentage of cells with the indicated phenotypes as measured by FACS.
  • Table 9B cells transduced with CARs have an effector memory phenotype.
  • CD3 (SEQ ID NO: 13)
  • CD45RO+/ CD45RO+/ CD45RO-/ CD45RO- CD62L+ CD62L- CD62L+ /CD62L- full length (f) CD27-CD3? 68.30 23.50 6.13 2.03 (SEQ ID NO: 7)
  • ACD27-4-1BB - ⁇ 3 ⁇ (SEQ 74.00 20.20 4.20 1.60 ID NO: 9)
  • Human T cells were transduced with an empty retroviral vector (MSGV1 ) or a retroviral vector encoding one of the constructs set forth in Table 9A.
  • Transduced cells were cultured alone (medium) or co-cultured with control target cells 624mel, 624/CD70, 938mel, or 938mel cells transduced to express CD70 (938/CD70) or RCC target cells RCC 2245R, RCC 2246R, RCC 2361 R, or RCC 1764. IFN- ⁇ secretion was measured. The results are shown in Figure 3.
  • human T cells transduced with ⁇ 0027- ⁇ 3 ⁇ (SEQ ID NO: 7), ACD27-4- l BB - ⁇ 3 ⁇ (SEQ ID NO: 9), ACD27-CD28 - 4-1 BB - € ⁇ ⁇ (SEQ ID NO: 10), fCD27-4-l BB - CD3 ⁇ (SEQ ID NO: 12), or fCD27-CD28 - 4- IBB - € ⁇ 3 (SEQ ID NO: 13) recognize CD70-expressing RCC tumor cells in vitro.
  • This example demonstrates the selection of a ACD27-4- 1 BB - ⁇ 3 ⁇ (SEQ ID NO: 9) retroviral-vector producing packaging clone.
  • Table 10 shows the percentage of cells with the indicated phenotypes as measured by FACS.
  • transduced clones were cultured alone (medium) or co-cultured with target control cells 938mel, 938/CD70, SNU l 079, SNU l 196, or target RCC cell lines RCC 2245R, RCC 2246R, RCC 2361 R, or RCC 1764. IFN- ⁇ secretion was measured. The results are shown in Figure 4. As shown in Figure 4, retroviral packaging clone E3 demonstrated reactivity against CD70-expressing target tumor cell lines.
  • Retroviral packaging cell clones were transduced with a CAR as set forth in Table 1 1 .
  • Table 1 1 shows the percentage of cells with the indicated phenotypes as measured by FACS. TABLE 1 1
  • transduced clones were cultured alone (medium) or co-cultured with target control cells 938mel, 938/CD70, SNU l 079, SNUl 196, or target RCC cell lines RCC 2245R, RCC 2246R, RCC 2361 R, or RCC 1764. IFN- ⁇ secretion was measured. The results are shown in Figure 5. As shown in Figure 5, retroviral packaging clone E3 demonstrated reactivity against CD70-expressing target tumor cell lines.

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105949325A (zh) * 2016-07-08 2016-09-21 重庆精准生物技术有限公司 包含cd27胞内结构域的嵌合抗原受体、慢病毒载体及其应用
WO2019051047A1 (en) * 2017-09-07 2019-03-14 University Of Florida Research Foundation, Inc. CHIMERIC ANTIGEN RECEPTOR T-LYMPHOCYTES EXPRESSING THE INTERLEUKIN-8 RECEPTOR
WO2019116046A1 (en) * 2017-12-15 2019-06-20 Autolus Limited Cell
WO2020108643A1 (en) * 2018-11-30 2020-06-04 Beijing Meikang Geno-Immune Biotechnology Co., Ltd. Cd19-and cd70-based combined car-t immunotherapy
EP3344263A4 (en) * 2016-08-04 2020-07-01 Memorial Sloan-Kettering Cancer Center CANCER ANTIGEN TARGETS AND USES THEREOF
US20200317807A1 (en) * 2014-12-08 2020-10-08 The United States Of America,As Represented By The Secretary,Department Of Health And Human Services Anti-cd70 chimeric antigen receptors
US20200384278A1 (en) * 2019-06-04 2020-12-10 Jerome Canady Research Institute for Advanced Biological and Technological Sciences Method for Combination Cold Atmospheric Plasma and CAR-T Therapy
WO2022129216A1 (en) 2020-12-15 2022-06-23 Universiteit Antwerpen Cell-based therapeutics targeting cd70
WO2022159791A1 (en) * 2021-01-25 2022-07-28 Board Of Regents, The University Of Texas System Cd27-extracellular domain car to target cd70-positive tumors
WO2022238963A3 (en) * 2021-05-12 2023-02-09 Crispr Therapeutics Ag Genetically engineered immune cells targeting cd70 for use in treating solid tumors
WO2023072307A1 (zh) * 2021-10-25 2023-05-04 重庆精准生物技术有限公司 一种靶向cd70的抗原结合片段、单链抗体和嵌合抗原受体及其应用
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CN112020518A (zh) 2018-02-01 2020-12-01 辉瑞公司 靶向cd70的嵌合抗原受体
JP7542441B2 (ja) * 2018-05-11 2024-08-30 クリスパー セラピューティクス アクチェンゲゼルシャフト 癌を治療するための方法及び組成物
KR20210038922A (ko) * 2018-08-02 2021-04-08 카이트 파마 인코포레이티드 키메라 항원 수용체 요법 t 세포 확장 동역학 및 그의 용도
EP3962498A4 (en) * 2019-04-30 2023-05-31 Memorial Sloan Kettering Cancer Center Combination therapies
MX2022008485A (es) * 2020-01-08 2022-08-02 Univ Texas Un metodo para modificar celulas asesinas naturales para dirigirse a tumores positivos a cd70.
CN111909966B (zh) * 2020-04-01 2021-09-21 苏州克睿基因生物科技有限公司 一种制备经修饰的免疫细胞的方法
AU2021377699A1 (en) 2020-11-13 2023-06-15 Catamaran Bio, Inc. Genetically modified natural killer cells and methods of use thereof
WO2022116952A1 (zh) * 2020-12-01 2022-06-09 苏州克睿基因生物科技有限公司 靶向cd70的抗原结合蛋白及其应用
CN117924489A (zh) * 2022-01-19 2024-04-26 上海恒润达生生物科技股份有限公司 抗cd70纳米抗体及其用途
JP2025511914A (ja) * 2022-04-07 2025-04-16 ボード オブ リージェンツ，ザ ユニバーシティ オブ テキサス システム 操作されたナチュラルキラー細胞の活性化および増殖方法と抗体との組み合わせ
CN117126856A (zh) * 2022-05-20 2023-11-28 上海雅科生物科技有限公司 以bcma胞外结构域为标记的基因、多肽、重组表达载体、基因工程化细胞及其应用
EP4572772A1 (en) 2022-08-17 2025-06-25 Capstan Therapeutics, Inc. Conditioning for in vivo immune cell engineering
US12311033B2 (en) 2023-05-31 2025-05-27 Capstan Therapeutics, Inc. Lipid nanoparticle formulations and compositions
US20250127728A1 (en) 2023-10-05 2025-04-24 Capstan Therapeutics, Inc. Constrained Ionizable Cationic Lipids and Lipid Nanoparticles
WO2025076113A1 (en) 2023-10-05 2025-04-10 Capstan Therapeutics, Inc. Ionizable cationic lipids with conserved spacing and lipid nanoparticles
US20250302763A1 (en) 2024-02-22 2025-10-02 Capstan Therapeutics, Inc. Immune engineering amplification
WO2025217452A1 (en) 2024-04-11 2025-10-16 Capstan Therapeutics, Inc. Constrained ionizable cationic lipids and lipid nanoparticles
WO2025217454A2 (en) 2024-04-11 2025-10-16 Capstan Therapeutics, Inc. Ionizable cationic lipids and lipid nanoparticles

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2012058460A2 (en) * 2010-10-27 2012-05-03 Baylor College Of Medicine Chimeric cd27 receptors for redirecting t cells to cd70-positive malignancies
WO2013185552A1 (zh) * 2012-06-12 2013-12-19 中国人民解放军第二军医大学东方肝胆外科医院 双信号独立的嵌合抗原受体及其用途

Family Cites Families (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1992001049A2 (en) * 1990-07-13 1992-01-23 The General Hospital Corporation Cd53 cell surface antigen and use thereof
US7285267B2 (en) * 1997-01-14 2007-10-23 Human Genome Sciences, Inc. Tumor necrosis factor receptors 6α & 6β
US20070037165A1 (en) * 2000-09-08 2007-02-15 Applera Corporation Polymorphisms in known genes associated with human disease, methods of detection and uses thereof
DK1545204T3 (en) 2002-09-06 2016-11-14 The Government Of The Us Secretary Dept Of Health And Human Services Immunotherapy with in vitro selected antigen-specific lymphocytes following non-myeloablative lymphodepletive chemotherapy
WO2008045437A2 (en) 2006-10-09 2008-04-17 The General Hospital Corporation Chimeric t-cell receptors and t-cells targeting egfrviii on tumors
US8383099B2 (en) 2009-08-28 2013-02-26 The United States Of America, As Represented By The Secretary, Department Of Health And Human Services Adoptive cell therapy with young T cells
EP2483301A1 (en) 2009-10-01 2012-08-08 The United States Of America, As Represented By The Secretary, Department of Health and Human Services Anti-vascular endothelial growth factor receptor-2 chimeric antigen receptors and use of same for the treatment of cancer
PH12013501201A1 (en) * 2010-12-09 2013-07-29 Univ Pennsylvania Use of chimeric antigen receptor-modified t cells to treat cancer
US20120244133A1 (en) 2011-03-22 2012-09-27 The United States of America, as represented by the Secretary, Department of Health and Methods of growing tumor infiltrating lymphocytes in gas-permeable containers
CN107188969B (zh) * 2011-04-08 2021-08-27 美国卫生和人力服务部 抗-表皮生长因子受体变体iii嵌合抗原受体及其用于治疗癌症的用途
WO2013059593A1 (en) 2011-10-20 2013-04-25 The United States Of America, As Represented By The Secretary, Department Of Health And Human Services Anti-cd22 chimeric antigen receptors
CA2863799C (en) 2012-02-22 2020-09-01 Matthew J. FRIGAULT Compositions and methods for generating a persisting population of t cells useful for the treatment of cancer
WO2014055771A1 (en) * 2012-10-05 2014-04-10 The Trustees Of The University Of Pennsylvania Human alpha-folate receptor chimeric antigen receptor
KR20210090298A (ko) * 2012-10-30 2021-07-19 에스퍼란스 파마슈티컬스, 인코포레이티드 항체/약물 컨쥬게이트 및 이의 사용 방법
CN104177499B (zh) * 2013-05-27 2019-01-08 上海雅科生物科技有限公司 一种嵌合抗原受体、编码基因、表达载体及其应用
JP6724009B2 (ja) * 2014-12-08 2020-07-15 アメリカ合衆国 抗ｃｄ７０キメラ抗原受容体

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2012058460A2 (en) * 2010-10-27 2012-05-03 Baylor College Of Medicine Chimeric cd27 receptors for redirecting t cells to cd70-positive malignancies
WO2013185552A1 (zh) * 2012-06-12 2013-12-19 中国人民解放军第二军医大学东方肝胆外科医院 双信号独立的嵌合抗原受体及其用途

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
DATABASE WPI Week 201405, Derwent World Patents Index; AN 2013-X28425, XP002742099 *
SHAFFER, D.R. ET AL.: "Foreign or Domestic CARs: Receptor Ligands as Antigen-Binding Domains", MEDICAL SCIENCES, vol. 2, no. 1, 28 January 2014 (2014-01-28), pages 23 - 36, XP002742098, DOI: 10.3390/medsci2010023 *

Cited By (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US11999796B2 (en) * 2014-12-08 2024-06-04 The United States Of America, As Represented By The Secretary, Department Of Health And Human Services Anti-CD70 chimeric antigen receptors
US20200317807A1 (en) * 2014-12-08 2020-10-08 The United States Of America,As Represented By The Secretary,Department Of Health And Human Services Anti-cd70 chimeric antigen receptors
CN105949325A (zh) * 2016-07-08 2016-09-21 重庆精准生物技术有限公司 包含cd27胞内结构域的嵌合抗原受体、慢病毒载体及其应用
CN105949325B (zh) * 2016-07-08 2019-07-16 重庆精准生物技术有限公司 包含cd27胞内结构域的嵌合抗原受体、慢病毒载体及其应用
US11193938B2 (en) 2016-08-04 2021-12-07 Memorial Sloan-Kettering Cancer Center Cancer antigen targets and uses thereof
EP3344263A4 (en) * 2016-08-04 2020-07-01 Memorial Sloan-Kettering Cancer Center CANCER ANTIGEN TARGETS AND USES THEREOF
US12345712B2 (en) 2016-08-04 2025-07-01 Memorial Sloan-Kettering Cancer Center Cancer antigen targets and uses thereof
US12259390B2 (en) 2016-08-04 2025-03-25 Memorial Sloan-Kettering Cancer Center Cancer antigen targets and uses thereof
WO2019051047A1 (en) * 2017-09-07 2019-03-14 University Of Florida Research Foundation, Inc. CHIMERIC ANTIGEN RECEPTOR T-LYMPHOCYTES EXPRESSING THE INTERLEUKIN-8 RECEPTOR
US11788093B2 (en) 2017-09-07 2023-10-17 University Of Florida Research Foundation, Inc. Chimeric antigen receptor t-cells expressing interleukin-8 receptor
CN111479918A (zh) * 2017-12-15 2020-07-31 奥托路斯有限公司 细胞
WO2019116046A1 (en) * 2017-12-15 2019-06-20 Autolus Limited Cell
EP4628503A3 (en) * 2017-12-15 2025-12-17 Autolus Limited Cell
US12304942B2 (en) 2017-12-15 2025-05-20 Autolus Limited Cell comprising a chimeric antigen receptor or a transgenic T-cell receptor and comprising a chimeric TNF receptor
WO2020108643A1 (en) * 2018-11-30 2020-06-04 Beijing Meikang Geno-Immune Biotechnology Co., Ltd. Cd19-and cd70-based combined car-t immunotherapy
US20200384278A1 (en) * 2019-06-04 2020-12-10 Jerome Canady Research Institute for Advanced Biological and Technological Sciences Method for Combination Cold Atmospheric Plasma and CAR-T Therapy
EP4031150A4 (en) * 2019-09-16 2023-11-01 The General Hospital Corporation CD70-DIRECTED CHIMERIC ANTIGEN RECEPTOR (CAR) T CELLS AND USES THEREOF
WO2022129216A1 (en) 2020-12-15 2022-06-23 Universiteit Antwerpen Cell-based therapeutics targeting cd70
EP4281483A4 (en) * 2021-01-25 2024-12-18 Board of Regents, The University of Texas System CD27 EXTRACELLULAR DOMAIN CAR TO TARGET CD70 POSITIVE TUMORS
WO2022159791A1 (en) * 2021-01-25 2022-07-28 Board Of Regents, The University Of Texas System Cd27-extracellular domain car to target cd70-positive tumors
WO2022238963A3 (en) * 2021-05-12 2023-02-09 Crispr Therapeutics Ag Genetically engineered immune cells targeting cd70 for use in treating solid tumors
WO2023072307A1 (zh) * 2021-10-25 2023-05-04 重庆精准生物技术有限公司 一种靶向cd70的抗原结合片段、单链抗体和嵌合抗原受体及其应用

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