TWI804044B - Btla同效劑抗體及其用途 - Google Patents
Btla同效劑抗體及其用途 Download PDFInfo
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- TWI804044B TWI804044B TW110141711A TW110141711A TWI804044B TW I804044 B TWI804044 B TW I804044B TW 110141711 A TW110141711 A TW 110141711A TW 110141711 A TW110141711 A TW 110141711A TW I804044 B TWI804044 B TW I804044B
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Abstract
本發明提供結合BTLA之抗體及使用其之方法,該等抗體適用作用於治療與自體免疫疾病相關聯之病況,包括治療狼瘡之藥劑。
Description
本發明屬醫學領域。更特定言之,本發明係關於針對B及T淋巴球衰減因子(BTLA)之抗體及其醫藥組合物。本發明之抗體期望適用於治療自身免疫疾病,諸如狼瘡。
狼瘡為具有異質特徵的自體免疫疾病,包括皮膚、口、肌肉及關節、心肌、周邊血液、肺、腎臟、生殖器官及CNS表現。狼瘡患者處於嚴重且危及生命的心臟血管、腎及神經精神疾病的風險下。標準護理包括大量類固醇,其具有許多不利及/或危險副作用。需要療法來控制疾病且允許減少或消除類固醇使用。
B及T淋巴球衰減因子(BTLA;CD272)為Ig超家族成員且為負調節免疫細胞活化之核查點受體家族的部分。BTLA主要表現於B細胞、T細胞及樹突狀細胞上。BTLA之天然配位體為TNF受體超家族成員,疱疹病毒條目介體(HVEM;TNFRSF14)。
據報導如藉由流式細胞量測術所偵測到的人類HVEM-Fc與表現於K
D為112 nM的293T細胞中之人類BTLA。(Cheung等人, PNAS, 2005年9月13日, 102:37;13218-13223)。使HVEM與BTLA結合使得酪胺酸磷酸化BTLA細胞質域上之兩個保守的基於免疫受體酪胺酸之抑制基元域。此磷酸化使得經由兩個Src同源性2域募集蛋白酪胺酸磷酸酶,所述蛋白酪胺酸磷酸酶藉由去磷酸化及下調陽性細胞受體信號傳導(例如,T細胞受體或B細胞受體信號轉導級聯)而賦予BTLA之抑制活性,因此使得抑制免疫細胞活化。在易於自發地出現狼瘡狀疾病之小鼠模型(MRL-lpr小鼠)中,相較於表現BTLA之小鼠,BTLA缺陷型小鼠在唾液腺、肺、胰腺、腎及關節中具有更嚴重淋巴球浸潤。因此,BTLA同效劑抗體可為患有自身免疫疾病(諸如狼瘡)之患者提供益處。
BTLA同效劑抗體為此項技術中已知的。舉例而言,美國專利第8,563,694號('694專利)揭示阻斷(Mab21H6及Mab19A7)或不阻斷(Mab8D5及Mab8A3)與BTLA結合之HVEM的BTLA同效劑抗體。'694專利描述對研發利用BTLA在淋巴球反應中的抑制性作用同時允許BTLA-HVEM結合之治療的持續需求。然而,缺乏模擬HVEM與BTLA之結合以用於治療自身免疫疾病的BTLA同效劑抗體。若抗體具有顯著重疊HVEM之結合位點的抗原決定基,則抗體「模擬」與BTLA結合之HVEM,且在抗體與HVEM之間存在結構類似性。亦缺乏結合人類BTLA且適用於研究自身免疫疾病之活體內臨床前模型(諸如鼠類及食蟹獼猴模型)的BTLA同效劑抗體。因此,仍存在對替代性BTLA同效劑抗體的需求。
本發明之抗體試圖提供替代性BTLA同效劑抗體。此等BTLA同效劑抗體可適用於治療自身免疫疾病,諸如狼瘡。此等BTLA同效劑抗體能夠結合來自多個物種之BTLA,諸如人類、食蟹獼猴及/或鼠類BTLA。另外,相較於具有與Mab8D5相同重鏈可變區及輕鏈可變區之抗體,此等BTLA同效劑抗體顯示增強的活體外活性。本發明之抗體具有此等所需特徵中之至少一者。
一個此類BTLA同效劑抗體能夠結合人類、食蟹獼猴及鼠類BTLA。出人意料地,由於此抗體模擬與BTLA結合之HVEM,因此其具有此所需交叉反應性。相較於結合BTLA之HVEM,此抗體亦對BTLA具有更高的結合親和力。此可為具有HVEM短暫水平之疾病狀態的患者提供益處,其中在患者HVEM降低的時間期間,可能需要具有攜帶模擬BTLA之同效劑抗體。
本發明提供與BTLA結合且活化及/或增強BTLA介導之信號傳導的抗體(BTLA同效劑抗體)。本發明提供一種抗體,其包含輕鏈可變區(LCVR)及重鏈可變區(HCVR),其中LCVR包含互補決定區(CDR) LCDR1、LCDR2及LCDR3且HCVR包含CDR HCDR1、HCDR2及HCDR3,且其中LCDR1之胺基酸序列為SEQ ID NO: 22,LCDR2之胺基酸序列為SEQ ID NO: 25,LCDR3之胺基酸序列為SEQ ID NO:28,HCDR1之胺基酸序列為SEQ ID NO: 13,HCDR2之胺基酸序列為SEQ ID NO: 16且HCDR3之胺基酸序列為SEQ ID NO: 19。在一實施例中,抗體包含LCVR及HCVR,且其中LCVR之胺基酸序列為SEQ ID NO: 4,且HCVR之胺基酸序列為SEQ ID NO: 3。在另一實施例中,抗體包含輕鏈(LC)及重鏈(HC),且其中LC之胺基酸序列為SEQ ID NO: 2,且HC之胺基酸序列為SEQ ID NO: 1。在又一實施例中,抗體包含2個LC及2個HC,其中各LC之胺基酸序列為SEQ ID NO: 2,且各HC之胺基酸序列為SEQ ID NO: 1。
本發明亦提供一種BTLA同效劑抗體,其中LCDR1之胺基酸序列為SEQ ID NO: 23,LCDR2之胺基酸序列為SEQ ID NO:26,LCDR3之胺基酸序列為SEQ ID NO: 29,HCDR1之胺基酸序列為SEQ ID NO: 14,HCDR2之胺基酸序列為SEQ ID NO: 17且HCDR3之胺基酸序列為SEQ ID NO: 20。在一實施例中,LCVR之胺基酸序列為SEQ ID NO: 8,且HCVR之胺基酸序列為SEQ ID NO: 7。在另一實施例中,LC之胺基酸序列為SEQ ID NO: 6,且HC之胺基酸序列為SEQ ID NO: 5。在又一實施例中,抗體包含2個LC及2個HC,其中各LC之胺基酸序列為SEQ ID NO: 6,且各HC之胺基酸序列為SEQ ID NO: 5。
本發明亦提供一種BTLA同效劑抗體,其中LCDR1之胺基酸序列為SEQ ID NO:24,LCDR2之胺基酸序列為SEQ ID NO:27,LCDR3之胺基酸序列為SEQ ID NO: 30,HCDR1之胺基酸序列為SEQ ID NO: 15,HCDR2之胺基酸序列為SEQ ID NO: 18且HCDR3之胺基酸序列為SEQ ID NO: 21。在一實施例中,LCVR之胺基酸序列為SEQ ID NO: 12,且HCVR之胺基酸序列為SEQ ID NO: 11。在另一實施例中,LC之胺基酸序列為SEQ ID NO: 10,且HC之胺基酸序列為SEQ ID NO: 9。在又一實施例中,抗體包含2個LC及2個HC,其中各LC之胺基酸序列為SEQ ID NO: 10,且各HC之胺基酸序列為SEQ ID NO: 9。
本發明亦提供一種結合BTLA之抗體,其中該抗體藉由包含以下之步驟產生:用人類BTLA之Fc標記之胞外域(ECD)域來使家兔免疫;及用人類及小鼠BTLA-Fc標記之蛋白質增強。人類BTLA ECD之胺基酸序列為SEQ ID NO: 31之胺基酸31-150。
本發明提供一種模擬與BTLA結合之HVEM之BTLA同效劑抗體。本發明亦提供一種BTLA同效劑抗體,其能夠結合人類、食蟹獼猴及鼠類BTLA。
本發明亦提供一種醫藥組合物,其包含本發明之抗體及一或多種醫藥學上可接受之載劑、稀釋劑或賦形劑。在一些實施例中,本發明之醫藥組合物可用於治療風濕性、神經性及皮膚病學疾病中之一或多者,從而此類治療包含向有需要之患者投與有效量之本發明之醫藥組合物。在一些特定實施例中,風濕性疾病為狼瘡性腎炎、全身性紅斑性狼瘡症及類風濕性關節炎中之至少一者。在其他特定實施例中,皮膚病學疾病為異位性皮膚炎及牛皮癬中之至少一者。在其他特定實施例中,神經性疾病為多發性硬化症。
本發明亦提供一種治療患有風濕性、神經性及皮膚病學疾病中之一或多者之患者的方法,該方法包含向有需要之患者投與有效量之本發明抗體。在一些此等實施例中,風濕性疾病為狼瘡性腎炎、全身性紅斑性狼瘡症及類風濕性關節炎中之至少一者。在其他特定實施例中,皮膚病學疾病為異位性皮膚炎及牛皮癬中之至少一者。在其他特定實施例中,神經性疾病為多發性硬化症。
本發明亦提供一種本發明之抗體或其醫藥組合物,以用於療法。在一些實施例中,本發明提供一種本發明之抗體或其醫藥組合物,以用於治療風濕性、神經性及皮膚病學疾病中之一或多者。在一些此等實施例中,風濕性疾病為狼瘡性腎炎、全身性紅斑性狼瘡症及類風濕性關節炎中之至少一者。在其他特定實施例中,皮膚病學疾病為異位性皮膚炎及牛皮癬中之至少一者。在其他特定實施例中,神經性疾病為多發性硬化症。
本發明亦提供本發明之抗體或其醫藥組合物的用途,其用於製造用於治療風濕性、神經性及皮膚病學疾病中之一或多者的藥劑。在一些此等實施例中,風濕性疾病為狼瘡性腎炎、全身性紅斑性狼瘡症及類風濕性關節炎中之至少一者。在其他特定實施例中,皮膚病學疾病為異位性皮膚炎及牛皮癬中之至少一者。在其他特定實施例中,神經性疾病為多發性硬化症。
本發明提供包含一種DNA分子,其包含編碼具有SEQ ID NO: 1、SEQ ID NO: 5或SEQ ID NO: 9之胺基酸序列之多肽的聚核苷酸序列。本發明亦提供一種DNA分子,其包含編碼具有SEQ ID NO: 2、SEQ ID NO: 6或SEQ ID NO: 10之胺基酸序列之多肽的聚核苷酸序列。
本發明提供一種DNA分子,其包含編碼具有SEQ ID NO: 1之胺基酸序列之多肽的聚核苷酸序列,且包含編碼具有SEQ ID NO: 2之胺基酸序列之多肽的聚核苷酸序列。本發明亦提供一種包含編碼具有SEQ ID NO: 1之胺基酸序列之多肽的聚核苷酸序列之DNA分子,及一種包含編碼具有SEQ ID NO: 2之胺基酸序列之多肽的聚核苷酸序列之DNA分子。在一特定實施例中,編碼具有SEQ ID NO: 1之胺基酸序列之多肽的聚核苷酸序列為SEQ ID NO:35且編碼具有SEQ ID NO: 2之胺基酸序列之多肽的聚核苷酸序列為SEQ ID NO:36。
本發明亦提供一種DNA分子,其包含編碼具有SEQ ID NO: 5之胺基酸序列之多肽的聚核苷酸序列,且包含編碼具有ID NO : 6之胺基酸序列之多肽的聚核苷酸序列。本發明亦提供一種包含編碼具有SEQ ID NO: 5之胺基酸序列之多肽的聚核苷酸序列之DNA分子,及一種包含編碼具有SEQ ID NO: 6之胺基酸序列之多肽的聚核苷酸序列之DNA分子。在一特定實施例中,編碼具有SEQ ID NO: 5之胺基酸序列之多肽的聚核苷酸序列為SEQ ID NO: 37,編碼具有SEQ ID NO: 6之胺基酸序列之多肽的聚核苷酸序列為SEQ ID NO: 38。
本發明亦提供一種DNA分子,其包含編碼具有SEQ ID NO: 9之胺基酸序列之多肽的聚核苷酸序列,且包含編碼具有SEQ ID NO: 10之胺基酸序列之多肽的聚核苷酸序列。本發明亦提供一種包含編碼具有SEQ ID NO: 9之胺基酸序列之多肽的聚核苷酸序列之DNA分子,及一種包含編碼具有SEQ ID NO: 10之胺基酸序列之多肽的聚核苷酸序列之DNA分子。在一特定實施例中,編碼具有SEQ ID NO: 9之胺基酸序列之多肽的聚核苷酸序列為SEQ ID NO: 39,編碼具有SEQ ID NO: 10之胺基酸序列之多肽的聚核苷酸序列為SEQ ID NO:40。
此外,本發明提供一種哺乳動物細胞,其包含:包含編碼具有SEQ ID NO: 1之胺基酸序列之多肽的聚核苷酸序列之DNA分子;及包含編碼具有SEQ ID NO: 2之胺基酸序列之多肽的聚核苷酸序列之DNA分子。本發明亦提供一種哺乳動物細胞,其包含DNA分子,該DNA分子包含編碼具有SEQ ID NO: 5之胺基酸序列之多肽及具有SEQ ID NO: 6之胺基酸序列之多肽的聚核苷酸序列。本發明亦提供一種哺乳動物細胞,其包含DNA分子,該DNA分子包含編碼具有SEQ ID NO: 9之胺基酸序列之多肽及具有SEQ ID NO: 10之胺基酸序列之多肽的聚核苷酸序列。在一實施例中,哺乳動物細胞株為中國倉鼠卵巢(Chinese Hamster Ovary;CHO)或倉鼠胚胎腎臟(Hamster embryonic kidney;HEK)細胞株。
本發明亦提供一種哺乳動物細胞,其包含:包含編碼具有SEQ ID NO: 1之胺基酸序列之多肽的聚核苷酸序列之DNA分子;及/或包含編碼具有SEQ ID NO: 2之胺基酸序列之多肽的聚核苷酸序列之DNA分子,其中該細胞能夠表現包含具有SEQ ID NO: 1之胺基酸序列之HC及具有SEQ ID NO: 2之胺基酸序列之LC的抗體。較佳地,哺乳動物細胞包含DNA分子,該DNA分子包含編碼具有SEQ ID NO: 1之胺基酸序列之多肽及具有SEQ ID NO: 2之胺基酸序列之多肽的聚核苷酸序列。在一實施例中,哺乳動物細胞株為CHO或HEK細胞株。
本發明亦提供一種哺乳動物細胞,其包含:包含編碼具有SEQ ID NO: 5之胺基酸序列之多肽的聚核苷酸序列之DNA分子;及/或包含編碼具有SEQ ID NO: 6之胺基酸序列之多肽的聚核苷酸序列之DNA分子,其中該細胞能夠表現包含具有SEQ ID NO: 5之胺基酸序列之HC及SEQ ID NO: 6之胺基酸序列之LC的抗體。較佳地,哺乳動物細胞包含DNA分子,該DNA分子包含編碼具有SEQ ID NO: 5之胺基酸序列之多肽及具有SEQ ID NO: 6之胺基酸序列之多肽的聚核苷酸序列。在一實施例中,哺乳動物細胞株為CHO或HEK細胞株。
本發明亦提供一種哺乳動物細胞,其包含:包含編碼具有SEQ ID NO: 9之胺基酸序列之多肽的聚核苷酸序列之DNA分子;及/或包含編碼具有SEQ ID NO: 10之胺基酸序列之多肽的聚核苷酸序列之DNA分子,其中該細胞能夠表現包含具有SEQ ID NO: 9之胺基酸序列之HC及具有SEQ ID NO: 10之胺基酸序列之LC的抗體。較佳地,哺乳動物細胞包含DNA分子,該DNA分子包含編碼具有SEQ ID NO: 9之胺基酸序列之多肽及具有SEQ ID NO: 10之胺基酸序列之多肽的聚核苷酸序列。在一實施例中,哺乳動物細胞株為CHO或HEK細胞株。
在另一實施例中,本發明提供一種用於產生抗體的方法,該抗體包含具有SEQ ID NO: 2之胺基酸序列的LC及具有SEQ ID NO: 1之胺基酸序列的HC,其中該方法包含:在使得抗體表現之條件下培育包含DNA之哺乳動物細胞,該DNA編碼具有SEQ ID NO: 2之胺基酸序列的LC及/或具有SEQ ID NO: 1之胺基酸序列的HC;及回收經表現抗體。本發明包括可藉由如上文剛剛描述之本發明方法獲得之抗體。
本發明亦提供一種用於產生抗體之方法,該抗體包含具有SEQ ID NO: 6之胺基酸序列的LC及具有SEQ ID NO: 5之胺基酸序列的HC,其中該方法包含:在使得抗體表現之條件下培育包含DNA之哺乳動物細胞,該DNA編碼具有SEQ ID NO: 6之胺基酸序列的LC及/或具有SEQ ID NO: 5之胺基酸序列的HC;及回收經表現抗體。本發明包括可藉由如上文剛剛描述之本發明方法獲得之抗體。
本發明亦提供一種用於產生抗體之方法,該抗體包含具有SEQ ID NO: 10之胺基酸序列的LC及具有SEQ ID NO: 9之胺基酸序列的HC,其中該方法包含:在使得抗體表現之條件下培育包含DNA之哺乳動物細胞,該DNA編碼具有SEQ ID NO: 10之胺基酸序列的LC及/或具有SEQ ID NO: 9之胺基酸序列的HC;及回收經表現抗體。本發明包括可藉由如上文剛剛描述之本發明方法獲得之抗體。
本發明包含一種用於產生抗體之方法,該抗體包含兩個HC及兩個LC,其中兩個HC中之每一者之胺基酸序列為SEQ ID NO: 1,且兩個LC中之每一者之胺基酸序列為SEQ ID NO: 2,且該方法包含:a)在使得抗體表現之條件下培育如上文所描述的本發明之哺乳動物細胞;及b)回收經表現抗體。本發明包括可藉由如上文剛剛描述之本發明方法獲得之抗體。
本發明亦包括一種用於產生抗體之方法,該抗體包含兩個HC及兩個LC,其中兩個HC中之每一者之胺基酸序列為SEQ ID NO: 5,且兩個LC中之每一者之胺基酸序列為SEQ ID NO: 6,且該方法包含:a)在使得抗體表現之條件下培育如上文所描述的本發明之哺乳動物細胞;及b)回收經表現抗體。本發明包括可藉由如上文剛剛描述之本發明方法獲得之抗體。
本發明亦包括一種用於產生抗體之方法,該抗體包含兩個HC及兩個LC,其中兩個HC中之每一者之胺基酸序列為SEQ ID NO: 9,且兩個LC中之每一者之胺基酸序列為SEQ ID NO: 10,且該方法包含:a)在使得抗體表現之條件下培育如上文所描述的本發明之哺乳動物細胞;及b)回收經表現抗體。本發明包括可藉由如上文剛剛描述之本發明方法獲得之抗體。
本發明提供一種抗體,其在具有以下SEQ ID NO: 31之殘基的結構性及功能性抗原決定基處接觸人類BTLA:位置42處之Arg及位置127處之His。本發明亦提供一種抗體,其在包含由SEQ ID NO: 31給出之胺基酸序列的位置42處之Arg的結構性及功能性抗原決定基處接觸人類BTLA。
本發明提供一種抗體,其在具有以下SEQ ID NO: 31之殘基的新穎結構性抗原決定基處接觸人類BTLA:位置35處之Asp、位置37處之Gln、位置42處之Arg、位置74處之Leu、位置76處之Gly、位置79處之Cys、位置114處之Arg、位置119處之Phe、位置120處之Gln、位置122處之Asn、位置128處之Ser。在一較佳實施例中,抗體22B3被稱為模擬與BTLA結合之HVEM,此係因為抗體22B3之HCDR3在結構上類似於HVEM。較佳地,當在諸如PyMOL™之程式中BTLA:抗體晶體結構與BTLA:HVEM晶體結構對齊時,抗體CDR環採用類似於HVEM環之構形,該HVEM環包含胺基酸殘基69至72 (SEQ ID NO:41之胺基酸ELTG)。
本發明提供一種抗體,其在功能性抗原決定基處接觸人類BTLA,該功能性抗原決定基具有SEQ ID NO: 31之位置52處之Asp。抗體接觸具有以下SEQ ID NO: 31之殘基的新穎結構性抗原決定基:位置46處之His、位置55處之Glu、位置103處之Glu、位置104處之Pro、位置106處之Leu、位置107處之Pro、位置134處之Thr、位置139處之Ala。
本發明提供一種抗體,其在功能性抗原決定基處接觸人類BTLA,該功能性抗原決定基具有SEQ ID NO: 31之位置68處之His及位置81處之Lys。在一實施例中,抗體接觸具有以下SEQ ID NO: 31之殘基的新穎結構性抗原決定基:位置62處之Tyr、位置64處之Ala、位置68處之His、位置85處之Arg、位置91處之Glu、位置98處之Phe、位置118處之Asn。
本發明提供一種抗體,其在具有以下SEQ ID NO: 31之殘基的新穎結構性抗原決定基處接觸人類BTLA:位置35處之Asp、位置37處之Gln、位置42處之Arg、位置74處之Leu、位置76處之Gly、位置79處之Cys、位置114處之Arg、位置119處之Phe、位置120處之Gln、位置122處之Asn以及位置124處之Ile、位置128處之Ser。
如本文中所使用,「抗體」為包含由二硫鍵互連之2個HC及2個LC的免疫球蛋白分子。各LC及HC之胺基末端部分包括約100-120個胺基酸之可變區,該可變區主要負責經由其中所含有之CDR識別抗原。CDR與稱為構架區(「FR」)之更保守之區穿插。各LCVR及HCVR由3個CDR及4個FR構成,其按以下順序自胺基末端至羧基末端排列:FR1、CDR1、FR2、CDR2、FR3、CDR3、FR4。LC之3個CDR稱為「LCDR1、LCDR2及LCDR3」,且HC之3個CDR稱為「HCDR1、HCDR2及HCDR3」。CDR含有與抗原形成特異性相互作用的大多數殘基。亦即,CDR含有與抗原之殘基接觸(在4.5Å內)的大多數殘基。因此,抗體結合特定抗原之功能性能力很大程度上受六個CDR內之胺基酸殘基影響。將胺基酸分配至本發明抗體之LCVR區及HCVR區內之CDR域係基於熟知Kabat編號慣例(Kabat等人, Ann. NY Acad. Sci. 190:382-93 (1971); Kabat等人, Sequences of Proteins of Immunological Interest, 第五版, 美國衛生及人類服務部(U.S.Department of Health and Human Services), NIH Publication第91-3242期(1991)),及Chothia (Chothia C, Lesk AM. Canonical structures for the hypervariable regions of immunoglobulins. J. Mol.Biol. 1987; 196:901-17. Chothia C, Lesk AM, Tramontano A, Levitt M, Smith-Gill SJ, Air G, Sheriff S, Padlan EA, Davies D, Tulip WR等人, Conformations of immunoglobulin hypervariable regions. Nature. 1989; 342:877-83)。HCDR1之起始胺基酸殘基由Chothia定義及HCDR1之末端胺基酸殘基由Kabat定義。HCDR2、HCDR3、LCDR1、LCDR2及LCDR3之起始胺基酸殘基及末端胺基酸殘基由Kabat定義。
如本文中所使用,術語「抗原決定基」可指結構性抗原決定基(與抗體之可變區接觸的抗原之位點)及/或功能性抗原決定基(可或可不與抗體之可變區接觸且對於抗體結合為必要的抗原之位點)。藉由X射線結晶學測定結構性抗原決定基,其中將經結合Fab上之另一個殘基之4.5Å內的人類BTLA上之任何殘基視為接觸位點。
本發明之抗體可使用已知方法製備及純化。舉例而言,編碼HC (例如由SEQ ID NO: 1給出之胺基酸序列)及LC (例如由SEQ ID NO: 2給出之胺基酸序列)之cDNA序列可經選殖且工程改造為GS(麩醯胺酸合成酶)表現載體。經工程改造的免疫球蛋白表現載體可隨後穩定轉染至CHO細胞中。如熟習此項技術者應瞭解,抗體之哺乳動物表現會引起糖基化,通常在Fc區中之極保守的N-糖基化位點處。穩定純系可經檢驗以用於表現與BTLA特異性結合之抗體。可將陽性純系擴增至無血清培養基中以用於在生物反應器中產生抗體。可藉由習知技術純化其中已分泌有抗體之培養基。舉例而言,可將培養基方便地施加至已用相容性緩衝液(諸如磷酸鹽緩衝鹽水)平衡之蛋白A或G瓊脂糖凝膠FF管柱。洗滌管柱以移除非特異性結合組分。例如藉由pH梯度溶離經結合的抗體,且諸如藉由SDS-PAGE偵測抗體溶離份且隨後彙集。可使用常見技術濃縮及/或無菌過濾抗體。可藉由常見技術(包括尺寸排阻、疏水性相互作用、離子交換或羥磷灰石層析)來有效移除可溶聚集體及多聚體。可在例如-70℃下將產物立即冷凍或可將其冷凍乾燥。
本發明之抗體可以併入至一種醫藥組合物中,該醫藥組合物可以藉由此項技術中熟知之方法製備且包含本發明之抗體及一或多種醫藥學上可接受之載劑、稀釋劑或賦形劑。
可藉由非經腸途徑(例如,皮下、靜脈內、腹膜內、肌肉內或經皮)向處於如本文所描述之疾病或病症風險下或呈現如本文所描述之疾病或病症之患者投與包含有效量之本發明抗體的醫藥組合物。「有效量」指達成所需治療結果所必需之量(在一定劑量下,及對於一定時間段而言,及對於投與方式而言)。抗體之有效量可根據諸如個體之疾病病況、年齡、性別及體重以及抗體引發個體中期望性反應之能力的因素而變化。有效量亦為本發明之抗體治療有利作用超過其任何毒性或不利作用的量。
本發明之抗體可用於治療患者。更特定言之,期望本發明之抗體治療風濕性、神經性及皮膚病學疾病中之一或多者。風濕性疾病之特徵為發炎,其可影響個人的關節、肌肉及/或器官。一種此類風濕性疾病為全身性紅斑性狼瘡症(SLE)。
如在本文中互換地使用,「治療(treatment)」及/或「治療(treating)」及/或「治療(treat)」旨在指其中可減緩、阻斷、遏制、控制、終止或逆轉本文所描述之病症之進展的所有方法,但未必表示完全消除所有病症症狀。治療包括投與本發明之抗體以用於治療將受益於BTLA活性增加之人類的疾病或病況且包括:(a)抑制疾病之進一步進展;及(b)緩解疾病,即使得疾病或病症消退或緩解其症狀或併發症。
抗體工程改造藉由用人類BTLA之Fc標記之胞外域(ECD)域來使家兔免疫且用小鼠BTLA-Fc標記之蛋白質(25F7)或替代地用人類及小鼠BTLA-Fc標記之蛋白期望(22B3及23C8)增強來產生本發明之抗體。藉由組胺酸標記之人類、小鼠及食蟹獼猴BTLA完成篩檢以鑑別交叉反應性。人類BTLA之胺基酸序列由SEQ ID NO: 31給出,Balbc小鼠BTLA之胺基酸序列由SEQ ID NO: 32給出,C57BL6之胺基酸序列由SEQ ID NO: 33給出,且食蟹獼猴BTLA之胺基酸序列由SEQ ID NO: 34給出。抗體隨後經人類化及且親和力成熟。
實例 工程改造之 BTLA 同效劑抗體之表現及純化本發明之BTLA同效劑抗體可基本如下表現及純化。可用分泌抗體之表現系統使用最佳的預定HC:LC載體比率(諸如1:3或1:2)或編碼HC及LC兩者之單個載體系統來瞬時或穩定地轉染合適宿主細胞(諸如HEK 293或CHO)。可使用許多常用技術中之任一種來純化其中已分泌有抗體的經澄清培養基。舉例而言,培養基可方便地施加至用相容性緩衝液(諸如磷酸鹽緩衝鹽水(pH 7.4))平衡的用於Fab片段之MabSelect管柱(GE Healthcare)或KappaSelect管柱(GE Healthcare)。可洗滌管柱以移除非特異性結合組分。可例如藉由pH梯度(諸如20 mM Tris緩衝液(pH 7.0)至10 mM檸檬酸鈉緩衝液(pH 3.0),或磷酸鹽緩衝鹽水(pH 7.4)至100 mM甘胺酸緩衝液(pH 3.0))溶離所結合的抗體。抗體溶離份可諸如藉由SDS-PAGE偵測且接著可經合併。視預期用途而定,進一步純化為視情況選用的。可使用常見技術濃縮及或無菌過濾抗體。可藉由常見技術(包括尺寸排阻、疏水性相互作用、離子交換、多模式或羥基磷灰石層析)來有效移除可溶性聚集物及多聚物。在此等層析步驟之後,抗體純度在約95%至約99%之間。產物可保持冷藏,在-70℃下立即冷凍,或可經冷凍乾燥。本發明之例示性抗體的胺基酸SEQ ID NO展示如下。
表 1 :例示性 BTLA 同效劑抗體之胺基酸序列。
抗體 SEQ ID NO | ||||||
抗體 | HCDR1 | HCDR2 | HCDR3 | LCDR1 | LCDR2 | LCDR3 |
22B3 | 13 | 16 | 19 | 22 | 25 | 28 |
23C8 | 14 | 17 | 20 | 23 | 26 | 29 |
25F7 | 15 | 18 | 21 | 24 | 27 | 30 |
結合親和力及動力學藉由表面電漿共振使用Biacore® 3000 (GE Healthcare)來量測本發明之BTLA同效劑抗體(22B3、23C8及25F7)對BTLA之結合親和力及動力學。藉由經由胺偶合將約120 RU BTLA蛋白質(人類、大鼠、鼠類(Balbc或C57BL6)或食蟹獼猴BTLA)固定於Biacore® CM5晶片上,且使BTLA同效劑抗體流動來量測結合親和力,自500 nM開始,在2倍連續稀釋中降至15.6 nM。實驗在25℃下在HBS-EP緩衝液(GE Healthcare BR100669;10 mM HEPES,150 mM NaCl,3 mM EDTA,0.05%界面活性劑P20,pH 7.4)中進行。對於各循環,250 μL之抗體樣品以50 μl/min流動穿過流動細胞1及2,且隨後解離10分鐘。藉由以10 μL/mL流速注射5 μL之pH 1.5之甘胺酸緩衝液來重新產生晶片表面。資料符合1:1朗謬爾結合模型(Langmiur binding model)以衍生kon、koff,並計算K
D。隨後程序基本上如上文所述,觀測到以下參數(展示於表2中)。下文所展示之資料為人類、食蟹獼猴、大鼠及鼠類對於22B3之三個實驗的平均值。
表 2 . 結合親和力及動力學。
如上文表2中所展示,本發明之BTLA同效劑抗體結合BTLA。特定言之,抗體22B3能夠結合人類、鼠類及獼猴BTLA。
抗體 | 抗原 ( BTLA ) | kon (1/Ms) | koff (1/s) | KD (nM) |
22B3 | 人類 | 5.87E+06 | 2.19E-03 | 0.365 |
食蟹獼猴 | 2.45E+06 | 6.47E-04 | 0.27 | |
鼠類 ( balbc ) | 2.60E+06 | 8.58E-02 | 32.5 | |
鼠類 (C57BL6) | 1.89E+06 | 2.65E-01 | 147 | |
大鼠 | 2.10E+06 | 4.62E-02 | 24.1 | |
23C8 | 人類 | 1.59E+05 | 2.93E-04 | 1.93 (n=3) |
食蟹獼猴 | 8.71E+04 | 3.09E-03 | 35.35 (n=2) | |
鼠類 (balbc) | 未結合 | 未結合 | 未結合 | |
鼠類 (C57BL6) | 未結合 | 未結合 | 未結合 | |
大鼠 | 未測試 | 未測試 | 未測試 | |
25F7 | 人類 | 6.8622E+04 | 1.42E-02 | 206.2 (n=2) |
食蟹獼猴 | 未測試 | 未測試 | 未測試 | |
鼠類 (balbc) | 未測試 | 未測試 | 未測試 | |
鼠類 (C57BL6) | 7.70E+04 | 3.50E-04 | 4.63 (n=1) | |
大鼠 | 未測試 | 未測試 | 未測試 |
結合初級細胞藉由FACS來測定本發明之BTLA抗體(22B3、23C8及25F7)結合來自不同物種之初級細胞的能力。根據製造商的協定,使用Ficoll (GE # 17-1440-02)及SepMate導管(STEMCELL # 15450)將人類周邊血液單核細胞(PBMC)自供體血液樣本(San Diego Blood Bank,# LRS-WBC)分離。食蟹獼猴PBMC (在世界範圍內的靈長類 # CA-10)自液氮解凍且用FACS緩衝液洗滌一次(與上文相同)。
來自雄性C57BL6小鼠(JAX)或雌性史泊格多利大鼠(Sprague Dawley rats) (Harlan)之脾臟經採集,合併且在用RPMI 1640沖洗之50 mL錐形管上使用細胞過濾器及注射器栓賽將其解離成單細胞懸浮液,用10%熱滅活FBS及2 mM EDTA完成。在用完全RPMI淬滅之前,粒化細胞、移除培養基,且藉由將丸粒再懸浮於2 ml ACK裂解緩衝液(gibco #A10492-01)中約2分鐘來來裂解紅細胞。裂解細胞可經粒化且以在FACS緩衝液(含有3% FBS、20 mM HEPES及2 mM EDTA之DPBS 1×)洗滌一次。
使用Countess細胞計數器定量經分離初級細胞,且以2×10
6個細胞/毫升再懸浮於FACS緩衝液中。在細胞分離的同一天藉由將50 µl (~0.1 × 10
6)個細胞接種至96孔盤(Greiner # 650101)中來執行流式細胞量測術實驗。藉由在4℃下添加1 µl Fc嵌段(例如,來自BD # 553142) 15分鐘且不洗滌來阻止非特異性抗體結合。
藉由在FACS緩衝液中連續稀釋,在不同濃度下測試BTLA抗體結合。舉例而言,以不同濃度開始之純化抗體及對照物首先稀釋至30 µg/mL且起始材料之連續1:3稀釋執行總共10次滴定(加上未處理對照物)。抗體滴定在4℃下與細胞一起培育20分鐘,並在染色之前用FACS緩衝液洗滌。細胞使用螢光染料共軛之抗體染色以鑑別特定細胞類型(例如,CD19 B細胞、CD4 T細胞或CD8 T細胞)或使用二級抗體染色以鑑別是否存在與子集結合之抗體。在流式細胞儀上分析之前,在4℃下執行染色20分鐘且用FACS緩衝液洗滌3次。結果使用標準FACS分析軟體(例如,FACSDiva)分析且報導為針對各滴定之二級抗體之平均螢光強度。藉由高於背景之平均螢光強度染色判定指示結合之陽性結果。
以下程序基本上如上文所描述,抗體22B3與人類、食蟹獼猴、大鼠及小鼠BTLA表現細胞結合,抗體23C8結合人類及食蟹獼猴BTLA表現細胞,且抗體25F7結合人類、食蟹獼猴及小鼠BTLA表現細胞。
BTLA 同效劑抗體誘導之磷酸化為測定本發明之BTLA同效劑抗體(22B3及25F7)在人類B細胞株中誘導酪胺酸磷酸化的能力,在37℃下以10 μg/mL將BTLA抗體結合至24孔培養盤一個小時。用PBS洗滌盤以移除任何未結合抗體。可以10×10
6個細胞/毫升將人類BTLA表現B細胞株(諸如Ramos.2G6.4C10人類B淋巴球細胞株(ATCC))添加至孔且在37℃下培育30 min。細胞經移除且裂解於完全裂解緩衝液(MSD)中,且在-80℃下冷凍至少30 min。
藉由Meso Sector S 600偵測到磷酸化BTLA。藉由在室溫下在阻斷溶液(MSD)中培育一小時來製備抗生蛋白鏈菌素偵測盤。在室溫下將生物素標記之BTLA捕捉抗體(5A5)塗佈至盤上一小時,隨後為三個或更多個Tris洗滌步驟。在室溫下培育細胞裂解物兩個小時。用SULFO-TAG抗BTLA抗體(ANC6E9)偵測到總BTLA,且用SULFO-TAG抗磷酸肌酐抗體(PY20;MSD),隨後三個或更多個Tris洗滌步驟來量測磷酸化BTLA。在使用Meso Sector S 600分析之前接著立即將2×讀取緩衝液T (MSD)添加物添加至孔。
以下程序基本上如上文所描述,抗體22B3使得背景下酪胺酸磷酸化BTLA相較於陰性對照增加2.41倍,且抗體25F7使得背景下酪胺酸磷酸化BTLA相較於陰性對照增加1.47倍。此等資料顯示BTLA同效劑抗體22B3及25F7能夠在人類B細胞株中誘導BTLA磷酸化。
抑制人類初級 B 細胞 增殖藉由抑制人類初級B細胞增殖之能力來評估本發明之BTLA同效劑抗體的活體外效能。使用人類B細胞分離套組(EasySep)自健康人類周邊血液單核細胞分離人類初級B細胞係且將其再懸浮於合適人類初級細胞培養基中。伴隨著滴定同型對照物或BTLA抗體將抗IgM塗佈至盤且在37℃下培育一個小時,隨後為PBS洗滌步驟。將經分離人類B細胞添加至各孔且在37℃下與5% CO
2一起培育72小時,隨後為[
3H]-胸苷脈衝最後18小時。移除培育後之盤且將其置放於乾冰上30分鐘且接著在-20℃下儲存直至準備好採集。細胞藉由解凍裂解且藉由Harvester9600(Tomtec)採集。藉由利用MicroBeta
22450微定量盤式計數器(Perkin Elmer)量測[
3H]-胸苷合併來評定增殖。
計數用於分析此分析中之相對增殖反應,且使用等式[抑制%=AVG最大信號-信號樣本)/AVG最大信號×100]來計算抑制百分比,該等式可用於使用繪圖軟體(GraphPad Prism)來測定IC50值。
以下程序基本上如上文所描述,BTLA同效劑抗體22B3能夠用經計算之0.32 + /-0.1 nM之IC50活體外抑制初級B細胞增殖,抗體23C8能夠用經計算之0.14 nM之IC50活體外抑制初級B細胞增殖,且抗體25F7能夠用經計算之0.17 nM之IC50活體外抑制初級B細胞增殖。在一類似實驗中,抗體22B3能夠用經計算之0.32 nM之IC50抑制初級B細胞增殖,且具有與Mab8D5相同的HCVR及LCVR (分別為'694專利之SEQ ID NO:11及18)之抗體用經計算之6.38 nM之IC50抑制初級B細胞增殖。此等資料顯示BTLA同效劑抗體22B3、23C8及25F7能夠活體外抑制B細胞增殖,且彼抗體22B3相較於Mab8D5具有更大的活體外活性。
GvHD 之人類化 NSG 小鼠模型活體內測定人類PBMC驅動之移植物抗宿主疾病(graft vs. host disease;GvHD)之預防。
簡言之,雌性NSG小鼠(JAX Labs,Stock # 05557) (約8-10週大)經標準化且基於基線體重量測值劃分為處理組(n=8小鼠/處理組)。根據製造商的協定,使用Ficoll (GE # 17-1440-02)及SepMate導管(STEMCELL # 15450)將人類周邊血液單核細胞(PBMC)自血液供體庫(San Diego Blood Bank,# LRS-WBC)分離。以大約150×10
6個細胞/毫升將PBMC再懸浮於PBS。處理組在給藥之前為不知情的。
在第1天,將懸浮於PBS (如上文所描述) (或用於非移植對照物之100 µl PBS)中之100 µl (15×10
6個細胞)之PBMC經靜脈內(IV)注至各小鼠之尾部中。藉由皮下(SQ)注射向小鼠每週給藥(QW)含呈不同濃度之本發明之抗體(22B3或23C8)或對照物之PBS媒劑。三個獨立研究係基本上如本文所描述執行三個獨立研究。用於各研究之給藥濃度為[研究1 (抗體22B3):0.1、1.0、5.0、10.0及20.0 mg/kg;研究2 (抗體22B3或23C8):0.001、0.01、10.0及100 mpk;以及研究3:0.001、0.005、0.01、0.1、0.5及1.0 mpk]。
終止研究,且在同型對照動物減重20%之前(研究1及2)或第28天(研究3),對小鼠進行安樂死。記錄體重(研究1及研究2),收集血清以用於細胞介素分析(研究1;藉由MSD ELISA執行分析;所分析細胞介素為TNFα、IL-10、IL-6、IL-4、IL12p70、IL-13、IL-2及IL-8),且採集脾臟以用於表型/藥力學分析(藉由CD 8 T細胞群的減少來量測;研究1及研究3)。
以下程序基本上如上文所述,獲得以下資料。
研究1中抗體22B3處理之動物顯示以下(呈0.1、1.0、5.0、10.0或20.0 mg/kg劑量之抗體):(i)在研究結束時,相較於未移植對照動物之體重,體重類似;(ii)相較於同型對照動物,細胞介素TNFα、IL-10、IL-6、IL-4及IL-12p70減少;以及(iii)相較於同型對照動物,CD 8 T細胞群減少(表型/藥力學分析)。
來自研究2之資料顯示在研究結束時,相較於未移植對照物動物之體重,經0.01 mg/kg抗體22B3,或1.0、5.0或10.0 mg/kg抗體23C8處理之小鼠具有類似體重。研究2未顯示22B3在10.0 mg/kg下對體重之活性,其可反映此模型之天然供體變化性。在研究3中,抗體22B3顯示呈以下劑量之抗體的活體內藥力學活性:0.01、0.1、0.5及1.0 mg/kg。綜合而言,此等資料顯示抗體22B3及抗體23C8有效活體內預防GvHD。
mIFNα 誘導之狼瘡性腎炎干擾素α (IFNα)誘導之狼瘡性腎炎模型為全身性紅斑性狼瘡症(SLE)之小鼠模型,其中IFNα用於與紐西蘭黑小鼠及紐西蘭白(NZB/W)小鼠雜交中同步發病且加速疾病進展。NZB/W小鼠模型為自發狼瘡性腎炎之經典模型。可使用腺病毒載體藉由外源性投與IFNα來加速此等小鼠體之疾病進展。此狼瘡性腎炎模型用於顯示本發明之BTLA同效劑抗體之活性。
研究開始前一天,基於體重隨機地分選十一週齡之雌性NZB/W小鼠。將小鼠分成以下處理組:(1)LacZ腺相關病毒AAV + 10 mg/kg人類IgG4 PAA同型對照(PAA為S228P、F234A及L235A突變);(2) IFNα AAV + 10 mg/kg人類IgG4 PAA同型對照;(3) IFNα AAV + 3 mg/kg22B3抗體;(4)IFNα AAV + 10 mg/kg 22B3抗體;或(5) IFNα AAV + 50 mg/kg環磷醯胺。在研究開始之日(第0天),小鼠經靜脈內一次投與含表現LacZ基因之AAV之10
11個基因組複本(GC) (未患病)或小鼠IFNα (患病)之PBS。在第1-4組中,自第0天開始每週一次經皮下用含同型對照或22B3抗體抗體之PBS處理小鼠。在第5組中,每10天腹膜內用含環磷醯胺之PBS處理小鼠。每2週自小鼠收集尿液樣本直至處理開始後6週研究終止。Kamiya Biomedical™小鼠微量白蛋白ELISA用於定量尿液白蛋白水平。藉由使用酶肌酐分析(Roche Diagnostics)來量測尿液肌酐。將白蛋白尿(腎功能之生物標記)定義為尿液中偵測到的每毫克肌酐大於300 µg白蛋白。
以下程序基本上如上文所描述,第4週,同型處理之患病組(IFNα AAV + hIgG4 PAA)中的白蛋白尿之發病率達到100%且保持升高直至研究結束,而LacZ AAV處理(非患病)之小鼠未展示任何白蛋白尿之發病率。可為急性腎毒性之環磷醯胺致使患病小鼠體內白蛋白尿瞬間增加,但環磷醯胺組中之白蛋白尿之發病率在研究結束時降至零。呈3 mg/kg及10 mg/kg之抗體22B3能夠在第28天時將白蛋白尿之發病率分別降至50%及20%,且在第42天時分別降至60%及70%。此等結果指示抗體22B3能夠保留模型的腎功能。
研究期間之卡普蘭-邁耶曲線圖(Kaplan-Meier plot) (資料未示)之存活%展示,同型處理之患病組之腎機能不全導致在第28天時開始死亡。研究結束之時,同型處理之患病組之存活率為60%。未患病且經環磷醯胺處理之組的存活率為100%。在研究結束之時,經10 mg/kg抗體22B3處理之小鼠亦展示100%存活率,而經3 mg/kg處理之小鼠展示80%存活率。此等結果指示抗體22B3能夠在此模型中預防疾病相關死亡。
牛皮癬之咪喹莫特誘導 ( Imiquimod-induced ) 之 模型測試本發明之抗體限制由施加TLR7/8同效劑咪喹莫特(IMQ)誘導之牛皮癬狀皮膚炎之嚴重程度的能力。在第0天時,七週齡雌性B6.SJL-
Ptprc a Pepc b/BoyJ小鼠(JAX庫存編號:002014)或HVEM
-/-小鼠(描述於Wang等人, J. Clin. Invest., 115:3, 711-717, 2005年3月中)分別腹膜內注射有3 mg/kg或1 mg/kg之抗體22B3或抗體25F7,且小鼠之背部經刮毛。注射有hIgG4同型對照之動物充當對照物。在第1-3天時,小鼠藉由吸入異氟醚(VetOne)麻醉,且接著將5% IMQ乳霜(50 mg,Fougera)塗覆至經刮毛皮膚之限定區域。在第4天時,切除皮膚之處理區域且分析疾病嚴重程度及發炎相關基因表現。
以下程序基本上如上文所描述,組織學分析顯示,在經hIgG4同型對照或1 mg/kg抗體22B3處理之組中,伴有角化不全及過度角化之表皮層增厚。經3 mg/kg抗體22B3或3 mg/kg抗體25F7處理之小鼠展示表皮厚度的明顯減小,其中一些區域呈現組織學正常。藉由qPCR使用iTaq Universal SYBR Green Supermix (Bio-Rad)分析在皮膚中之基因表現。經3 mg/kg抗體22B3處理之小鼠展現類型I IFN (IFNα、IFNβ)及IFNγ,以及IFN反應基因(Isg15、Mx1、Mx2、Oas2)表現的顯著減少。對涉及建立IMQ誘導之皮炎的細胞介素之分析亦顯示3 mg/kg抗體22B3處理組中IL-22及IL-23表現的顯著減少。此等資料顯示BTLA同效劑抗體22B3及25F7能夠減小牛皮癬狀皮膚炎之小鼠模型的表皮厚度。
抗原決定基測定藉由ELISA測定本發明之BTLA同效劑抗體之功能性抗原決定基,且藉由X射線結晶學測定結構性抗原決定基。
方法 ELISA : 功能性抗原決定基將以下一組BTLA之表面突變組單獨地引入至稠合到(人類)Fc之人類BTLA蛋白中:D35R、Q37R、Y39E、R42D、Q43A、E45R、S47H、L49R、D52R、E55R、E57R、D84R、N65R、H68A、V80R、K81E、E83R、S88H、K90H、E91H、I95R、E103H、L106R、N108R、R114V、S121Y、N122R、E125H、H127E、T130R、Y132R及T134H。
使用ELISA測定22B3及23C8之結合,其中待繪製抗原決定基之抗體由固定化抗家兔抗體捕獲,且在洗滌之後,將各BTLA突變體與所捕獲抗體培育為4點4倍稀釋系列且用酶聯抗人類Fc試劑偵測。將所得信號在抗體與對照抗體之間進行比較。功能性抗原決定基通常藉由針對一個或兩個突變體之信號的顯著減少來指示自身。對於25F7抗體,執行夾層ELISA,其中固定人類化22B3,BTLA突變體經捕獲且由家兔25F7結合。此得到更強的信號且可在消除22B3抗原決定基之後鑑別25F7抗原決定基。
X 射線結晶學: 結構性抗原決定基為測定各種抗體之相互作用介面且因此BTLA上之物理抗原決定基,人類BTLA與本發明抗體之Fab部分共結晶且測定晶體結構。根據所得晶體結構,將任何抗體原子之4.5Å內的BTLA殘基視為抗原決定基之部分(使用Pymol目測軟體)。自原子中心至原子中心量測為4.5埃。具有至少一個原子(亦即接近抗體中之任何原子4.5埃)之任何殘基為抗原決定基之部分。
在具有人類BTLA之複合物中測定兩個22B3結構。首先利用親本家兔22B3抗體Fab,組胺酸經標記且用表現為Fc融合體之人類BTLA之S47H突變體(穩定突變體)純化,且接著分解及純化。此兩種蛋白以大約等莫耳比混合且在可商購的篩網中篩檢以用於結晶。獲得晶體且在高階光子源極(Advanced Photon Source)處收集繞射資料。此資料藉由分子置換減少並解決且經改進以得到在22B3與BTLA之間的複合物的高解析度結構。第二複合物在人類化22B3 (Fab部分)之親和力成熟版本(具有HC突變I56Q/T57H/G98A及LC S95H)與人類BTLA之間。此等經共表現,純化為複合物並進行類似地篩檢。所得結構及抗原決定基類似於第一結構。
以與第一22B3複合物相同之方式,亦即藉由純化His標記之家兔親本Fab,與單體S47H人類BTLA混合及結晶來獲得含23C8結構之複合物。
根據第二22B3複合物,亦即藉由共表現、共純化及結晶來獲得具有人類BTLA之含25F7結構之複合物。利用具有與人類BTLA之經改良結合的人類化25F7之雙突變體(用於抗原決定基測定之人類化25F7在HC S30W/LC E27R處具有突變體)。
結果 22B3 抗體:在一組BTLA表面突變體中,R42D及H127E對與家兔22B3抗體(包含與22B3相同但具有家兔架構之CDR)結合具有顯著負面影響。功能性抗原決定基包含人類BTLA (SEQ ID NO:31)之位置42處之Arg及位置127處之His。人類BTLA與家兔22B3 Fab之間的晶體結構複合物中之22B3之4.5埃內且為結構性抗原決定基的BTLA殘基為以下SEQ ID NO: 31之殘基:位置35處之Asp、位置37處之Gln、位置42處之Arg、位置74處之Leu、位置76處之Gly、位置79處之Cys、位置114處之Arg、位置119處之Phe、位置120處之Gln以及位置122處之Asn、位置128處之Ser。人類BTLA與人類22B3變體(HC I56Q/T57H/G98A LC S95H) Fab之間的晶體結構複合物中之22B3之4.5埃內的BTLA殘基為SEQ ID NO: 31之位置35處之Asp、位置37處之Gln、位置42處之Arg、位置74處之Leu、位置76處之Gly、位置79處之Cys、位置114處之Arg、位置119處之Phe、位置120處之Gln、位置122處之Asn以及位置124處之Ile、位置128處之Ser。
在類似研究中,用於結合BTLA之HVEM的結構性抗原決定基為以下BTLA之胺基酸:位置37處之Gln、位置42處之Arg、位置74處之Leu、位置76處之Gly、位置77處之Thr、位置112處之Ser、位置114處之Arg、位置118處之Asn、位置121處之Ser、位置128處之Ser以及位置130處之Thr。藉由將抗體:BTLA晶體結構疊加至對準BTLA分子之HVEM:BTLA晶體結構上來評定抗體22B3與HVEM之間的結構類似性。含有胺基酸殘基69-72之HVEM區及對應抗體區之主鏈均方根偏差經測定為1.4埃。
23C8 抗體:D52R在ELISA中阻斷家兔23C8 (包含與23C8相同之HCDR1、HCDR2、HCDR3、LCDR1及LCDR2,具有QCTYGGVVGSTSDDNP之LCDR3且具有家兔架構)與人類BTLA之結合。功能性抗原決定基包含人類BTLA (SEQ ID NO:31)之位置52處之Asp。人類BTLA (S47H)與家兔23C8 Fab之間的晶體結構複合物中之23C8之4.5埃內且為結構性抗原決定基的BTLA殘基為SEQ ID NO: 31之位置46處之His、位置55處之Glu、位置103處之Glu、位置104處之Pro、位置106處之Leu、位置107處之Pro、位置134處之Thr以及位置139處之Ala。抗體23C8不模擬HVEM結合。
25F7 抗體:在一組BTLA表面突變體中,H68A及K61E對與家兔25F7抗體(包含與25F7相同但具有家兔架構之CDR)結合具有顯著負面影響。功能性抗原決定基包含人類BTLA (SEQ ID NO:31)之位置68處之His及位置81處之Lys。人類BTLA與人類化25F7 Fab變體(HC S30W,LC E27R)之間的晶體結構複合物中之25F7之4.5埃內且為結構性抗原決定基的BTLA殘基為SEQ ID NO: 31之位置62處之Tyr、位置64處之Ala、位置68處之His、位置85處之Arg、位置91處之Glu、位置98處之Phe以及位置118處之Asn。抗體25F7不模擬HVEM結合。
<![CDATA[<110> 美商美國禮來大藥廠(Eli Lilly and Company)]]> <![CDATA[<120> BTLA同效劑抗體及其用途]]> <![CDATA[<130> TW107115166]]> <![CDATA[<130> TW108133289]]> <![CDATA[<150> US 62/508510]]> <![CDATA[<151> 2017-05-19]]> <![CDATA[<160> 41 ]]> <![CDATA[<170> PatentIn version 3.5]]> <![CDATA[<210> 1]]> <![CDATA[<211> 449]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> 合成構築體]]> <![CDATA[<400> 1]]> Gln Val Gln Leu Val Gln Ser Gly Ala Glu Val Lys Lys Pro Gly Ala 1 5 10 15 Ser Val Lys Val Ser Cys Lys Ala Ser Gly Phe Ser Leu Ser Ser Tyr 20 25 30 Gly Val Ser Trp Val Arg Gln Ala Pro Gly Gln Gly Leu Glu Trp Met 35 40 45 Gly Ala Ile Ser Tyr Asp Gly Ile Thr Tyr Tyr Ala Ser Trp Ala Lys 50 55 60 Ser Arg Val Thr Met Thr Arg Asp Thr Ser Thr Ser Thr Val Tyr Met 65 70 75 80 Glu Leu Ser Ser Leu Arg Ser Glu Asp Thr Ala Val Tyr Tyr Cys Ala 85 90 95 Arg Gly Asp Tyr Tyr Asp Asp Tyr Val Tyr Val Tyr Ala Leu Asp Ile 100 105 110 Trp Gly Gln Gly Thr Leu Val Thr Val Ser Ser Ala Ser Thr Lys Gly 115 120 125 Pro Ser Val Phe Pro Leu Ala Pro Cys Ser Arg Ser Thr Ser Glu Ser 130 135 140 Thr Ala Ala Leu Gly Cys Leu Val Lys Asp Tyr Phe Pro Glu Pro Val 145 150 155 160 Thr Val Ser Trp Asn Ser Gly Ala Leu Thr Ser Gly Val His Thr Phe 165 170 175 Pro Ala Val Leu Gln Ser Ser Gly Leu Tyr Ser Leu Ser Ser Val Val 180 185 190 Thr Val Pro Ser Ser Ser Leu Gly Thr Lys Thr Tyr Thr Cys Asn Val 195 200 205 Asp His Lys Pro Ser Asn Thr Lys Val Asp Lys Arg Val Glu Ser Lys 210 215 220 Tyr Gly Pro Pro Cys Pro Pro Cys Pro Ala Pro Glu Ala Ala Gly Gly 225 230 235 240 Pro Ser Val Phe Leu Phe Pro Pro Lys Pro Lys Asp Thr Leu Met Ile 245 250 255 Ser Arg Thr Pro Glu Val Thr Cys Val Val Val Asp Val Ser Gln Glu 260 265 270 Asp Pro Glu Val Gln Phe Asn Trp Tyr Val Asp Gly Val Glu Val His 275 280 285 Asn Ala Lys Thr Lys Pro Arg Glu Glu Gln Phe Asn Ser Thr Tyr Arg 290 295 300 Val Val Ser Val Leu Thr Val Leu His Gln Asp Trp Leu Asn Gly Lys 305 310 315 320 Glu Tyr Lys Cys Lys Val Ser Asn Lys Gly Leu Pro Ser Ser Ile Glu 325 330 335 Lys Thr Ile Ser Lys Ala Lys Gly Gln Pro Arg Glu Pro Gln Val Tyr 340 345 350 Thr Leu Pro Pro Ser Gln Glu Glu Met Thr Lys Asn Gln Val Ser Leu 355 360 365 Thr Cys Leu Val Lys Gly Phe Tyr Pro Ser Asp Ile Ala Val Glu Trp 370 375 380 Glu Ser Asn Gly Gln Pro Glu Asn Asn Tyr Lys Thr Thr Pro Pro Val 385 390 395 400 Leu Asp Ser Asp Gly Ser Phe Phe Leu Tyr Ser Arg Leu Thr Val Asp 405 410 415 Lys Ser Arg Trp Gln Glu Gly Asn Val Phe Ser Cys Ser Val Met His 420 425 430 Glu Ala Leu His Asn His Tyr Thr Gln Lys Ser Leu Ser Leu Ser Leu 435 440 445 Gly <![CDATA[<210> 2]]> <![CDATA[<211> 217]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> 合成構築體]]> <![CDATA[<400> 2]]> Glu Ile Val Leu Thr Gln Ser Pro Gly Thr Leu Ser Leu Ser Pro Gly 1 5 10 15 Glu Arg Ala Thr Leu Ser Cys Gln Ala Ser Gln Ser Ile Ser Thr Ala 20 25 30 Leu Ala Trp Tyr Gln Gln Lys Pro Gly Gln Ala Pro Arg Leu Leu Ile 35 40 45 Tyr Ala Ala Ser Thr Leu Ala Ser Gly Ile Pro Asp Arg Phe Ser Gly 50 55 60 Ser Gly Ser Gly Thr Asp Phe Thr Leu Thr Ile Ser Arg Leu Glu Pro 65 70 75 80 Glu Asp Phe Ala Val Tyr Tyr Cys Gln Gln Gly Tyr Ser Ser Ser Asn 85 90 95 Leu Asp Asn Val Phe Gly Gly Gly Thr Lys Val Glu Ile Lys Arg Thr 100 105 110 Val Ala Ala Pro Ser Val Phe Ile Phe Pro Pro Ser Asp Glu Gln Leu 115 120 125 Lys Ser Gly Thr Ala Ser Val Val Cys Leu Leu Asn Asn Phe Tyr Pro 130 135 140 Arg Glu Ala Lys Val Gln Trp Lys Val Asp Asn Ala Leu Gln Ser Gly 145 150 155 160 Asn Ser Gln Glu Ser Val Thr Glu Gln Asp Ser Lys Asp Ser Thr Tyr 165 170 175 Ser Leu Ser Ser Thr Leu Thr Leu Ser Lys Ala Asp Tyr Glu Lys His 180 185 190 Lys Val Tyr Ala Cys Glu Val Thr His Gln Gly Leu Ser Ser Pro Val 195 200 205 Thr Lys Ser Phe Asn Arg Gly Glu Cys 210 215 <![CDATA[<210> 3]]> <![CDATA[<211> 123]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> 合成構築體]]> <![CDATA[<400> 3]]> Gln Val Gln Leu Val Gln Ser Gly Ala Glu Val Lys Lys Pro Gly Ala 1 5 10 15 Ser Val Lys Val Ser Cys Lys Ala Ser Gly Phe Ser Leu Ser Ser Tyr 20 25 30 Gly Val Ser Trp Val Arg Gln Ala Pro Gly Gln Gly Leu Glu Trp Met 35 40 45 Gly Ala Ile Ser Tyr Asp Gly Ile Thr Tyr Tyr Ala Ser Trp Ala Lys 50 55 60 Ser Arg Val Thr Met Thr Arg Asp Thr Ser Thr Ser Thr Val Tyr Met 65 70 75 80 Glu Leu Ser Ser Leu Arg Ser Glu Asp Thr Ala Val Tyr Tyr Cys Ala 85 90 95 Arg Gly Asp Tyr Tyr Asp Asp Tyr Val Tyr Val Tyr Ala Leu Asp Ile 100 105 110 Trp Gly Gln Gly Thr Leu Val Thr Val Ser Ser 115 120 <![CDATA[<210> 4]]> <![CDATA[<211> 110]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> 合成構築體]]> <![CDATA[<400> 4]]> Glu Ile Val Leu Thr Gln Ser Pro Gly Thr Leu Ser Leu Ser Pro Gly 1 5 10 15 Glu Arg Ala Thr Leu Ser Cys Gln Ala Ser Gln Ser Ile Ser Thr Ala 20 25 30 Leu Ala Trp Tyr Gln Gln Lys Pro Gly Gln Ala Pro Arg Leu Leu Ile 35 40 45 Tyr Ala Ala Ser Thr Leu Ala Ser Gly Ile Pro Asp Arg Phe Ser Gly 50 55 60 Ser Gly Ser Gly Thr Asp Phe Thr Leu Thr Ile Ser Arg Leu Glu Pro 65 70 75 80 Glu Asp Phe Ala Val Tyr Tyr Cys Gln Gln Gly Tyr Ser Ser Ser Asn 85 90 95 Leu Asp Asn Val Phe Gly Gly Gly Thr Lys Val Glu Ile Lys 100 105 110 <![CDATA[<210> 5]]> <![CDATA[<211> 441]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> 合成構築體]]> <![CDATA[<400> 5]]> Glu Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Pro Gly Gly 1 5 10 15 Ser Leu Arg Leu Ser Cys Ala Ala Ser Gly Phe Asp Ile Ser Lys Tyr 20 25 30 Asn Ile Gln Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Val 35 40 45 Gly Phe Ile Asn Tyr Gly Gly Ser Ala Tyr Tyr Ala Ser Arg Ala Lys 50 55 60 Gly Arg Phe Thr Ile Ser Arg Asp Asp Ser Lys Asn Ser Leu Tyr Leu 65 70 75 80 Gln Met Asn Ser Leu Lys Thr Glu Asp Thr Ala Val Tyr Tyr Cys Ala 85 90 95 Arg Gly Leu Ser Asn Ser Asp Leu Trp Gly Gln Gly Thr Leu Val Thr 100 105 110 Val Ser Ser Ala Ser Thr Lys Gly Pro Ser Val Phe Pro Leu Ala Pro 115 120 125 Cys Ser Arg Ser Thr Ser Glu Ser Thr Ala Ala Leu Gly Cys Leu Val 130 135 140 Lys Asp Tyr Phe Pro Glu Pro Val Thr Val Ser Trp Asn Ser Gly Ala 145 150 155 160 Leu Thr Ser Gly Val His Thr Phe Pro Ala Val Leu Gln Ser Ser Gly 165 170 175 Leu Tyr Ser Leu Ser Ser Val Val Thr Val Pro Ser Ser Ser Leu Gly 180 185 190 Thr Lys Thr Tyr Thr Cys Asn Val Asp His Lys Pro Ser Asn Thr Lys 195 200 205 Val Asp Lys Arg Val Glu Ser Lys Tyr Gly Pro Pro Cys Pro Pro Cys 210 215 220 Pro Ala Pro Glu Ala Ala Gly Gly Pro Ser Val Phe Leu Phe Pro Pro 225 230 235 240 Lys Pro Lys Asp Thr Leu Met Ile Ser Arg Thr Pro Glu Val Thr Cys 245 250 255 Val Val Val Asp Val Ser Gln Glu Asp Pro Glu Val Gln Phe Asn Trp 260 265 270 Tyr Val Asp Gly Val Glu Val His Asn Ala Lys Thr Lys Pro Arg Glu 275 280 285 Glu Gln Phe Asn Ser Thr Tyr Arg Val Val Ser Val Leu Thr Val Leu 290 295 300 His Gln Asp Trp Leu Asn Gly Lys Glu Tyr Lys Cys Lys Val Ser Asn 305 310 315 320 Lys Gly Leu Pro Ser Ser Ile Glu Lys Thr Ile Ser Lys Ala Lys Gly 325 330 335 Gln Pro Arg Glu Pro Gln Val Tyr Thr Leu Pro Pro Ser Gln Glu Glu 340 345 350 Met Thr Lys Asn Gln Val Ser Leu Thr Cys Leu Val Lys Gly Phe Tyr 355 360 365 Pro Ser Asp Ile Ala Val Glu Trp Glu Ser Asn Gly Gln Pro Glu Asn 370 375 380 Asn Tyr Lys Thr Thr Pro Pro Val Leu Asp Ser Asp Gly Ser Phe Phe 385 390 395 400 Leu Tyr Ser Arg Leu Thr Val Asp Lys Ser Arg Trp Gln Glu Gly Asn 405 410 415 Val Phe Ser Cys Ser Val Met His Glu Ala Leu His Asn His Tyr Thr 420 425 430 Gln Lys Ser Leu Ser Leu Ser Leu Gly 435 440 <![CDATA[<210> 6]]> <![CDATA[<211> 221]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> 合成構築體]]> <![CDATA[<400> 6]]> Asp Ile Gln Met Thr Gln Ser Pro Ser Ser Leu Ser Ala Ser Val Gly 1 5 10 15 Asp Arg Val Thr Ile Thr Cys Gln Ala Ser Gln Ser Ile Ser Ser Trp 20 25 30 Leu Ser Trp Tyr Gln Gln Lys Pro Gly Lys Ala Pro Lys Leu Leu Ile 35 40 45 Tyr Arg Ala Ser Thr Leu Ala Ser Gly Val Pro Ser Arg Phe Ser Gly 50 55 60 Ser Gly Ser Gly Thr Asp Phe Thr Phe Thr Ile Ser Ser Leu Gln Pro 65 70 75 80 Glu Asp Ile Ala Thr Tyr Tyr Cys Gln Ser Thr Tyr Gly Gly Val Val 85 90 95 Gly Ser Thr Ser Asp Asp Asn Pro Phe Gly Gly Gly Thr Lys Val Glu 100 105 110 Ile Lys Arg Thr Val Ala Ala Pro Ser Val Phe Ile Phe Pro Pro Ser 115 120 125 Asp Glu Gln Leu Lys Ser Gly Thr Ala Ser Val Val Cys Leu Leu Asn 130 135 140 Asn Phe Tyr Pro Arg Glu Ala Lys Val Gln Trp Lys Val Asp Asn Ala 145 150 155 160 Leu Gln Ser Gly Asn Ser Gln Glu Ser Val Thr Glu Gln Asp Ser Lys 165 170 175 Asp Ser Thr Tyr Ser Leu Ser Ser Thr Leu Thr Leu Ser Lys Ala Asp 180 185 190 Tyr Glu Lys His Lys Val Tyr Ala Cys Glu Val Thr His Gln Gly Leu 195 200 205 Ser Ser Pro Val Thr Lys Ser Phe Asn Arg Gly Glu Cys 210 215 220 <![CDATA[<210> 7]]> <![CDATA[<211> 115]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> 合成構築體]]> <![CDATA[<400> 7]]> Glu Val Gln Leu Val Glu Ser Gly Gly Gly Leu Val Gln Pro Gly Gly 1 5 10 15 Ser Leu Arg Leu Ser Cys Ala Ala Ser Gly Phe Asp Ile Ser Lys Tyr 20 25 30 Asn Ile Gln Trp Val Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Val 35 40 45 Gly Phe Ile Asn Tyr Gly Gly Ser Ala Tyr Tyr Ala Ser Arg Ala Lys 50 55 60 Gly Arg Phe Thr Ile Ser Arg Asp Asp Ser Lys Asn Ser Leu Tyr Leu 65 70 75 80 Gln Met Asn Ser Leu Lys Thr Glu Asp Thr Ala Val Tyr Tyr Cys Ala 85 90 95 Arg Gly Leu Ser Asn Ser Asp Leu Trp Gly Gln Gly Thr Leu Val Thr 100 105 110 Val Ser Ser 115 <![CDATA[<210> 8]]> <![CDATA[<211> 114]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> 合成構築體]]> <![CDATA[<400> 8]]> Asp Ile Gln Met Thr Gln Ser Pro Ser Ser Leu Ser Ala Ser Val Gly 1 5 10 15 Asp Arg Val Thr Ile Thr Cys Gln Ala Ser Gln Ser Ile Ser Ser Trp 20 25 30 Leu Ser Trp Tyr Gln Gln Lys Pro Gly Lys Ala Pro Lys Leu Leu Ile 35 40 45 Tyr Arg Ala Ser Thr Leu Ala Ser Gly Val Pro Ser Arg Phe Ser Gly 50 55 60 Ser Gly Ser Gly Thr Asp Phe Thr Phe Thr Ile Ser Ser Leu Gln Pro 65 70 75 80 Glu Asp Ile Ala Thr Tyr Tyr Cys Gln Ser Thr Tyr Gly Gly Val Val 85 90 95 Gly Ser Thr Ser Asp Asp Asn Pro Phe Gly Gly Gly Thr Lys Val Glu 100 105 110 Ile Lys <![CDATA[<210> 9]]> <![CDATA[<211> 447]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> 合成構築體]]> <![CDATA[<400> 9]]> Gln Val Gln Leu Val Gln Ser Gly Ala Glu Val Lys Lys Pro Gly Ala 1 5 10 15 Ser Val Lys Val Ser Cys Lys Ala Ser Gly Phe Ser Leu Ser Thr Tyr 20 25 30 Ala Met Asn Trp Val Arg Gln Ala Pro Gly Gln Gly Leu Glu Trp Met 35 40 45 Gly Ile Ile Ser Asp Asp Gly Thr Thr Tyr Tyr Ala Thr Trp Ala Lys 50 55 60 Gly Arg Val Thr Met Thr Arg Asp Thr Ser Thr Ser Thr Val Tyr Met 65 70 75 80 Glu Leu Ser Ser Leu Arg Ser Glu Asp Thr Ala Val Tyr Tyr Cys Ala 85 90 95 Arg Asp Ala Gly Ala Gly Gly Val Gln Asp Tyr Leu Thr Leu Trp Gly 100 105 110 Gln Gly Thr Leu Val Thr Val Ser Ser Ala Ser Thr Lys Gly Pro Ser 115 120 125 Val Phe Pro Leu Ala Pro Cys Ser Arg Ser Thr Ser Glu Ser Thr Ala 130 135 140 Ala Leu Gly Cys Leu Val Lys Asp Tyr Phe Pro Glu Pro Val Thr Val 145 150 155 160 Ser Trp Asn Ser Gly Ala Leu Thr Ser Gly Val His Thr Phe Pro Ala 165 170 175 Val Leu Gln Ser Ser Gly Leu Tyr Ser Leu Ser Ser Val Val Thr Val 180 185 190 Pro Ser Ser Ser Leu Gly Thr Lys Thr Tyr Thr Cys Asn Val Asp His 195 200 205 Lys Pro Ser Asn Thr Lys Val Asp Lys Arg Val Glu Ser Lys Tyr Gly 210 215 220 Pro Pro Cys Pro Pro Cys Pro Ala Pro Glu Ala Ala Gly Gly Pro Ser 225 230 235 240 Val Phe Leu Phe Pro Pro Lys Pro Lys Asp Thr Leu Met Ile Ser Arg 245 250 255 Thr Pro Glu Val Thr Cys Val Val Val Asp Val Ser Gln Glu Asp Pro 260 265 270 Glu Val Gln Phe Asn Trp Tyr Val Asp Gly Val Glu Val His Asn Ala 275 280 285 Lys Thr Lys Pro Arg Glu Glu Gln Phe Asn Ser Thr Tyr Arg Val Val 290 295 300 Ser Val Leu Thr Val Leu His Gln Asp Trp Leu Asn Gly Lys Glu Tyr 305 310 315 320 Lys Cys Lys Val Ser Asn Lys Gly Leu Pro Ser Ser Ile Glu Lys Thr 325 330 335 Ile Ser Lys Ala Lys Gly Gln Pro Arg Glu Pro Gln Val Tyr Thr Leu 340 345 350 Pro Pro Ser Gln Glu Glu Met Thr Lys Asn Gln Val Ser Leu Thr Cys 355 360 365 Leu Val Lys Gly Phe Tyr Pro Ser Asp Ile Ala Val Glu Trp Glu Ser 370 375 380 Asn Gly Gln Pro Glu Asn Asn Tyr Lys Thr Thr Pro Pro Val Leu Asp 385 390 395 400 Ser Asp Gly Ser Phe Phe Leu Tyr Ser Arg Leu Thr Val Asp Lys Ser 405 410 415 Arg Trp Gln Glu Gly Asn Val Phe Ser Cys Ser Val Met His Glu Ala 420 425 430 Leu His Asn His Tyr Thr Gln Lys Ser Leu Ser Leu Ser Leu Gly 435 440 445 <![CDATA[<210> 10]]> <![CDATA[<211> 217]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> 合成構築體]]> <![CDATA[<400> 10]]> Asp Ile Val Met Thr Gln Ser Pro Asp Ser Leu Ala Val Ser Leu Gly 1 5 10 15 Glu Arg Ala Thr Ile Asn Cys Gln Ala Ser Glu Asn Ile Tyr Asn Phe 20 25 30 Leu Ala Trp Tyr Gln Gln Lys Pro Gly Gln Pro Pro Lys Leu Leu Ile 35 40 45 Tyr Ser Ala Ser Thr Leu Ala Ser Gly Val Pro Asp Arg Phe Ser Gly 50 55 60 Ser Gly Ser Gly Thr Asp Phe Thr Leu Thr Ile Ser Ser Leu Gln Ala 65 70 75 80 Glu Asp Val Ala Val Tyr Tyr Cys Gln Gln Gly Ser Ser Asn Ser Asn 85 90 95 Ile Asp Asn Pro Phe Gly Gly Gly Thr Lys Val Glu Ile Lys Arg Thr 100 105 110 Val Ala Ala Pro Ser Val Phe Ile Phe Pro Pro Ser Asp Glu Gln Leu 115 120 125 Lys Ser Gly Thr Ala Ser Val Val Cys Leu Leu Asn Asn Phe Tyr Pro 130 135 140 Arg Glu Ala Lys Val Gln Trp Lys Val Asp Asn Ala Leu Gln Ser Gly 145 150 155 160 Asn Ser Gln Glu Ser Val Thr Glu Gln Asp Ser Lys Asp Ser Thr Tyr 165 170 175 Ser Leu Ser Ser Thr Leu Thr Leu Ser Lys Ala Asp Tyr Glu Lys His 180 185 190 Lys Val Tyr Ala Cys Glu Val Thr His Gln Gly Leu Ser Ser Pro Val 195 200 205 Thr Lys Ser Phe Asn Arg Gly Glu Cys 210 215 <![CDATA[<210> 11]]> <![CDATA[<211> 121]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> 合成構築體]]> <![CDATA[<400> 11]]> Gln Val Gln Leu Val Gln Ser Gly Ala Glu Val Lys Lys Pro Gly Ala 1 5 10 15 Ser Val Lys Val Ser Cys Lys Ala Ser Gly Phe Ser Leu Ser Thr Tyr 20 25 30 Ala Met Asn Trp Val Arg Gln Ala Pro Gly Gln Gly Leu Glu Trp Met 35 40 45 Gly Ile Ile Ser Asp Asp Gly Thr Thr Tyr Tyr Ala Thr Trp Ala Lys 50 55 60 Gly Arg Val Thr Met Thr Arg Asp Thr Ser Thr Ser Thr Val Tyr Met 65 70 75 80 Glu Leu Ser Ser Leu Arg Ser Glu Asp Thr Ala Val Tyr Tyr Cys Ala 85 90 95 Arg Asp Ala Gly Ala Gly Gly Val Gln Asp Tyr Leu Thr Leu Trp Gly 100 105 110 Gln Gly Thr Leu Val Thr Val Ser Ser 115 120 <![CDATA[<210> 12]]> <![CDATA[<211> 110]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> 合成構築體]]> <![CDATA[<400> 12]]> Asp Ile Val Met Thr Gln Ser Pro Asp Ser Leu Ala Val Ser Leu Gly 1 5 10 15 Glu Arg Ala Thr Ile Asn Cys Gln Ala Ser Glu Asn Ile Tyr Asn Phe 20 25 30 Leu Ala Trp Tyr Gln Gln Lys Pro Gly Gln Pro Pro Lys Leu Leu Ile 35 40 45 Tyr Ser Ala Ser Thr Leu Ala Ser Gly Val Pro Asp Arg Phe Ser Gly 50 55 60 Ser Gly Ser Gly Thr Asp Phe Thr Leu Thr Ile Ser Ser Leu Gln Ala 65 70 75 80 Glu Asp Val Ala Val Tyr Tyr Cys Gln Gln Gly Ser Ser Asn Ser Asn 85 90 95 Ile Asp Asn Pro Phe Gly Gly Gly Thr Lys Val Glu Ile Lys 100 105 110 <![CDATA[<210> 13]]> <![CDATA[<211> 10]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> 合成構築體]]> <![CDATA[<400> 13]]> Gly Phe Ser Leu Ser Ser Tyr Gly Val Ser 1 5 10 <![CDATA[<210> 14]]> <![CDATA[<211> 10]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> 合成構築體]]> <![CDATA[<400> 14]]> Gly Phe Asp Ile Ser Lys Tyr Asn Ile Gln 1 5 10 <![CDATA[<210> 15]]> <![CDATA[<211> 10]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> 合成構築體]]> <![CDATA[<400> 15]]> Gly Phe Ser Leu Ser Thr Tyr Ala Met Asn 1 5 10 <![CDATA[<210> 16]]> <![CDATA[<211> 16]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> 合成構築體]]> <![CDATA[<400> 16]]> Ala Ile Ser Tyr Asp Gly Ile Thr Tyr Tyr Ala Ser Trp Ala Lys Ser 1 5 10 15 <![CDATA[<210> 17]]> <![CDATA[<211> 16]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> 合成構築體]]> <![CDATA[<400> 17]]> Phe Ile Asn Tyr Gly Gly Ser Ala Tyr Tyr Ala Ser Arg Ala Lys Gly 1 5 10 15 <![CDATA[<210> 18]]> <![CDATA[<211> 16]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> 合成構築體]]> <![CDATA[<400> 18]]> Ile Ile Ser Asp Asp Gly Thr Thr Tyr Tyr Ala Thr Trp Ala Lys Gly 1 5 10 15 <![CDATA[<210> 19]]> <![CDATA[<211> 15]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> 合成構築體]]> <![CDATA[<400> 19]]> Gly Asp Tyr Tyr Asp Asp Tyr Val Tyr Val Tyr Ala Leu Asp Ile 1 5 10 15 <![CDATA[<210> 20]]> <![CDATA[<211> 7]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> 合成構築體]]> <![CDATA[<400> 20]]> Gly Leu Ser Asn Ser Asp Leu 1 5 <![CDATA[<210> 21]]> <![CDATA[<211> 13]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> 合成構築體]]> <![CDATA[<400> 21]]> Asp Ala Gly Ala Gly Gly Val Gln Asp Tyr Leu Thr Leu 1 5 10 <![CDATA[<210> 22]]> <![CDATA[<211> 11]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> 合成構築體]]> <![CDATA[<400> 22]]> Gln Ala Ser Gln Ser Ile Ser Thr Ala Leu Ala 1 5 10 <![CDATA[<210> 23]]> <![CDATA[<211> 11]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> 合成構築體]]> <![CDATA[<400> 23]]> Gln Ala Ser Gln Ser Ile Ser Ser Trp Leu Ser 1 5 10 <![CDATA[<210> 24]]> <![CDATA[<211> 11]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> 合成構築體]]> <![CDATA[<400> 24]]> Gln Ala Ser Glu Asn Ile Tyr Asn Phe Leu Ala 1 5 10 <![CDATA[<210> 25]]> <![CDATA[<211> 7]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> 合成構築體]]> <![CDATA[<400> 25]]> Ala Ala Ser Thr Leu Ala Ser 1 5 <![CDATA[<210> 26]]> <![CDATA[<211> 7]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> 合成構築體]]> <![CDATA[<400> 26]]> Arg Ala Ser Thr Leu Ala Ser 1 5 <![CDATA[<210> 27]]> <![CDATA[<211> 7]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> 合成構築體]]> <![CDATA[<400> 27]]> Ser Ala Ser Thr Leu Ala Ser 1 5 <![CDATA[<210> 28]]> <![CDATA[<211> 12]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> 合成構築體]]> <![CDATA[<400> 28]]> Gln Gln Gly Tyr Ser Ser Ser Asn Leu Asp Asn Val 1 5 10 <![CDATA[<210> 29]]> <![CDATA[<211> 16]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> 合成構築體]]> <![CDATA[<400> 29]]> Gln Ser Thr Tyr Gly Gly Val Val Gly Ser Thr Ser Asp Asp Asn Pro 1 5 10 15 <![CDATA[<210> 30]]> <![CDATA[<211> 12]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> 合成構築體]]> <![CDATA[<400> 30]]> Gln Gln Gly Ser Ser Asn Ser Asn Ile Asp Asn Pro 1 5 10 <![CDATA[<210> 31]]> <![CDATA[<211> 289]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 智人]]> <![CDATA[<400> 31]]> Met Lys Thr Leu Pro Ala Met Leu Gly Thr Gly Lys Leu Phe Trp Val 1 5 10 15 Phe Phe Leu Ile Pro Tyr Leu Asp Ile Trp Asn Ile His Gly Lys Glu 20 25 30 Ser Cys Asp Val Gln Leu Tyr Ile Lys Arg Gln Ser Glu His Ser Ile 35 40 45 Leu Ala Gly Asp Pro Phe Glu Leu Glu Cys Pro Val Lys Tyr Cys Ala 50 55 60 Asn Arg Pro His Val Thr Trp Cys Lys Leu Asn Gly Thr Thr Cys Val 65 70 75 80 Lys Leu Glu Asp Arg Gln Thr Ser Trp Lys Glu Glu Lys Asn Ile Ser 85 90 95 Phe Phe Ile Leu His Phe Glu Pro Val Leu Pro Asn Asp Asn Gly Ser 100 105 110 Tyr Arg Cys Ser Ala Asn Phe Gln Ser Asn Leu Ile Glu Ser His Ser 115 120 125 Thr Thr Leu Tyr Val Thr Asp Val Lys Ser Ala Ser Glu Arg Pro Ser 130 135 140 Lys Asp Glu Met Ala Ser Arg Pro Trp Leu Leu Tyr Arg Leu Leu Pro 145 150 155 160 Leu Gly Gly Leu Pro Leu Leu Ile Thr Thr Cys Phe Cys Leu Phe Cys 165 170 175 Cys Leu Arg Arg His Gln Gly Lys Gln Asn Glu Leu Ser Asp Thr Ala 180 185 190 Gly Arg Glu Ile Asn Leu Val Asp Ala His Leu Lys Ser Glu Gln Thr 195 200 205 Glu Ala Ser Thr Arg Gln Asn Ser Gln Val Leu Leu Ser Glu Thr Gly 210 215 220 Ile Tyr Asp Asn Asp Pro Asp Leu Cys Phe Arg Met Gln Glu Gly Ser 225 230 235 240 Glu Val Tyr Ser Asn Pro Cys Leu Glu Glu Asn Lys Pro Gly Ile Val 245 250 255 Tyr Ala Ser Leu Asn His Ser Val Ile Gly Pro Asn Ser Arg Leu Ala 260 265 270 Arg Asn Val Lys Glu Ala Pro Thr Glu Tyr Ala Ser Ile Cys Val Arg 275 280 285 Ser <![CDATA[<210> 32]]> <![CDATA[<211> 306]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 小家鼠]]> <![CDATA[<400> 32]]> Met Lys Thr Val Pro Ala Met Leu Gly Thr Pro Arg Leu Phe Arg Glu 1 5 10 15 Phe Phe Ile Leu His Leu Gly Leu Trp Ser Ile Leu Cys Glu Lys Ala 20 25 30 Thr Lys Arg Asn Asp Glu Glu Cys Glu Val Gln Leu Asn Ile Lys Arg 35 40 45 Asn Ser Lys His Ser Ala Trp Thr Gly Glu Leu Phe Lys Ile Glu Cys 50 55 60 Pro Val Lys Tyr Cys Val His Arg Pro Asn Val Thr Trp Cys Lys His 65 70 75 80 Asn Gly Thr Ile Trp Val Pro Leu Glu Val Gly Pro Gln Leu Tyr Thr 85 90 95 Ser Trp Glu Glu Asn Arg Ser Val Pro Val Phe Val Leu His Phe Lys 100 105 110 Pro Ile His Leu Ser Asp Asn Gly Ser Tyr Ser Cys Ser Thr Asn Phe 115 120 125 Asn Ser Gln Val Ile Asn Ser His Ser Val Thr Ile His Val Arg Glu 130 135 140 Arg Thr Gln Asn Ser Ser Glu His Pro Leu Ile Thr Val Ser Asp Ile 145 150 155 160 Pro Asp Ala Thr Asn Ala Ser Gly Pro Ser Thr Met Glu Glu Arg Pro 165 170 175 Gly Arg Thr Trp Leu Leu Tyr Thr Leu Leu Pro Leu Gly Ala Leu Leu 180 185 190 Leu Leu Leu Ala Cys Val Cys Leu Leu Cys Phe Leu Lys Arg Ile Gln 195 200 205 Gly Lys Glu Lys Lys Pro Ser Asp Leu Ala Gly Arg Asp Thr Asn Leu 210 215 220 Val Asp Ile Pro Ala Ser Ser Arg Thr Asn His Gln Ala Leu Pro Ser 225 230 235 240 Gly Thr Gly Ile Tyr Asp Asn Asp Pro Trp Ser Ser Met Gln Asp Glu 245 250 255 Ser Glu Leu Thr Ile Ser Leu Gln Ser Glu Arg Asn Asn Gln Gly Ile 260 265 270 Val Tyr Ala Ser Leu Asn His Cys Val Ile Gly Arg Asn Pro Arg Gln 275 280 285 Glu Asn Asn Met Gln Glu Ala Pro Thr Glu Tyr Ala Ser Ile Cys Val 290 295 300 Arg Ser 305 <![CDATA[<210> 33]]> <![CDATA[<211> 306]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 小家鼠]]> <![CDATA[<400> 33]]> Met Lys Thr Val Pro Ala Met Leu Gly Thr Pro Arg Leu Phe Arg Glu 1 5 10 15 Phe Phe Ile Leu His Leu Gly Leu Trp Ser Ile Leu Cys Glu Lys Ala 20 25 30 Thr Lys Arg Asn Asp Glu Glu Cys Pro Val Gln Leu Thr Ile Thr Arg 35 40 45 Asn Ser Lys Gln Ser Ala Arg Thr Gly Glu Leu Phe Lys Ile Gln Cys 50 55 60 Pro Val Lys Tyr Cys Val His Arg Pro Asn Val Thr Trp Cys Lys His 65 70 75 80 Asn Gly Thr Ile Cys Val Pro Leu Glu Val Ser Pro Gln Leu Tyr Thr 85 90 95 Ser Trp Glu Glu Asn Gln Ser Val Pro Val Phe Val Leu His Phe Lys 100 105 110 Pro Ile His Leu Ser Asp Asn Gly Ser Tyr Ser Cys Ser Thr Asn Phe 115 120 125 Asn Ser Gln Val Ile Asn Ser His Ser Val Thr Ile His Val Thr Glu 130 135 140 Arg Thr Gln Asn Ser Ser Glu His Pro Leu Ile Thr Val Ser Asp Ile 145 150 155 160 Pro Asp Ala Thr Asn Ala Ser Gly Pro Ser Thr Met Glu Glu Arg Pro 165 170 175 Gly Arg Thr Trp Leu Leu Tyr Thr Leu Leu Pro Leu Gly Ala Leu Leu 180 185 190 Leu Leu Leu Ala Cys Val Cys Leu Leu Cys Phe Leu Lys Arg Ile Gln 195 200 205 Gly Lys Glu Lys Lys Pro Ser Asp Leu Ala Gly Arg Asp Thr Asn Leu 210 215 220 Val Asp Ile Pro Ala Ser Ser Arg Thr Asn His Gln Ala Leu Pro Ser 225 230 235 240 Gly Thr Gly Ile Tyr Asp Asn Asp Pro Trp Ser Ser Met Gln Asp Glu 245 250 255 Ser Glu Leu Thr Ile Ser Leu Gln Ser Glu Arg Asn Asn Gln Gly Ile 260 265 270 Val Tyr Ala Ser Leu Asn His Cys Val Ile Gly Arg Asn Pro Arg Gln 275 280 285 Glu Asn Asn Met Gln Glu Ala Pro Thr Glu Tyr Ala Ser Ile Cys Val 290 295 300 Arg Ser 305 <![CDATA[<210> 34]]> <![CDATA[<211> 289]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 食蟹獼猴]]> <![CDATA[<400> 34]]> Met Lys Thr Leu Pro Ala Met Leu Gly Ser Gly Arg Leu Phe Trp Val 1 5 10 15 Val Phe Leu Ile Pro Tyr Leu Asp Ile Trp Asn Ile His Gly Lys Glu 20 25 30 Ser Cys Asp Val Gln Leu Tyr Ile Lys Arg Gln Ser Tyr His Ser Ile 35 40 45 Phe Ala Gly Asp Pro Phe Lys Leu Glu Cys Pro Val Lys Tyr Cys Ala 50 55 60 His Arg Pro Gln Val Thr Trp Cys Lys Leu Asn Gly Thr Thr Cys Val 65 70 75 80 Lys Leu Glu Gly Arg His Thr Ser Trp Lys Gln Glu Lys Asn Leu Ser 85 90 95 Phe Phe Ile Leu His Phe Glu Pro Val Leu Pro Ser Asp Asn Gly Ser 100 105 110 Tyr Arg Cys Ser Ala Asn Phe Leu Ser Ala Ile Ile Glu Ser His Ser 115 120 125 Thr Thr Leu Tyr Val Thr Asp Val Lys Ser Ala Ser Glu Arg Pro Ser 130 135 140 Lys Asp Glu Met Ala Ser Arg Pro Trp Leu Leu Tyr Ser Leu Leu Pro 145 150 155 160 Leu Gly Gly Leu Pro Leu Leu Ile Thr Thr Cys Phe Cys Leu Phe Cys 165 170 175 Phe Leu Arg Arg His Gln Gly Lys Gln Asn Glu Leu Ser Asp Thr Thr 180 185 190 Gly Arg Glu Ile Thr Leu Val Asp Val Pro Phe Lys Ser Glu Gln Thr 195 200 205 Glu Ala Ser Thr Arg Gln Asn Ser Gln Val Leu Leu Ser Glu Thr Gly 210 215 220 Ile Tyr Asp Asn Glu Pro Asp Phe Cys Phe Arg Met Gln Glu Gly Ser 225 230 235 240 Glu Val Tyr Ser Asn Pro Cys Leu Glu Glu Asn Lys Pro Gly Ile Ile 245 250 255 Tyr Ala Ser Leu Asn His Ser Ile Ile Gly Leu Asn Ser Arg Gln Ala 260 265 270 Arg Asn Val Lys Glu Ala Pro Thr Glu Tyr Ala Ser Ile Cys Val Arg 275 280 285 Ser <![CDATA[<210> 35]]> <![CDATA[<211> 1347]]> <![CDATA[<212> DNA]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> 合成構築體]]> <![CDATA[<400> 35]]> caggtgcagc tggtgcagtc tggggctgag gtgaagaagc ctggggcctc agtgaaggtt 60 tcctgcaagg catctggatt ctccctcagt agctatggag tgagctgggt gcgacaggcc 120 cctggacaag ggcttgagtg gatgggagcc attagttatg atggtattac atactacgcg 180 agctgggcga aaagcagagt caccatgacc agggacacgt ccacgagcac agtctacatg 240 gagctgagca gcctgagatc tgaggacacg gccgtgtatt actgtgcgag aggggactac 300 tacgatgatt atgtttatgt ttatgcttta gacatctggg gccagggcac cctggtcacc 360 gtctcctcag cttctaccaa gggcccatcg gtcttcccgc tagcgccctg ctccaggagc 420 acctccgaga gcacagccgc cctgggctgc ctggtcaagg actacttccc cgaaccggtg 480 acggtgtcgt ggaactcagg cgccctgacc agcggcgtgc acaccttccc ggctgtccta 540 cagtcctcag gactctactc cctcagcagc gtggtgaccg tgccctccag cagcttgggc 600 acgaagacct acacctgcaa cgtagatcac aagcccagca acaccaaggt ggacaagaga 660 gttgagtcca aatatggtcc cccatgccca ccctgcccag cacctgaggc cgccggggga 720 ccatcagtct tcctgttccc cccaaaaccc aaggacactc tcatgatctc ccggacccct 780 gaggtcacgt gcgtggtggt ggacgtgagc caggaagacc ccgaggtcca gttcaactgg 840 tacgtggatg gcgtggaggt gcataatgcc aagacaaagc cgcgggagga gcagttcaac 900 agcacgtacc gtgtggtcag cgtcctcacc gtcctgcacc aggactggct gaacggcaag 960 gagtacaagt gcaaggtctc caacaaaggc ctcccgtcct ccatcgagaa aaccatctcc 1020 aaagccaaag ggcagccccg agagccacag gtgtacaccc tgcccccatc ccaggaggag 1080 atgaccaaga accaggtcag cctgacctgc ctggtcaaag gcttctaccc cagcgacatc 1140 gccgtggagt gggaaagcaa tgggcagccg gagaacaact acaagaccac gcctcccgtg 1200 ctggactccg acggctcctt cttcctctac agcaggctaa ccgtggacaa gagcaggtgg 1260 caggagggga atgtcttctc atgctccgtg atgcatgagg ctctgcacaa ccactacaca 1320 cagaagagcc tctccctgtc tctgggt 1347 <![CDATA[<210> 36]]> <![CDATA[<211> 651]]> <![CDATA[<212> DNA]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> 合成構築體]]> <![CDATA[<400> 36]]> gaaattgtgt tgacgcagtc tccaggcacc ctgtctttgt ctccagggga aagagccacc 60 ctctcctgcc aggccagtca gagcattagt actgcattag cctggtacca gcagaaacct 120 ggccaggctc ccaggctcct catctatgct gcatccactc tggcatctgg catcccagac 180 aggttcagtg gcagtgggtc tgggacagac ttcactctca ccatcagcag actggagcct 240 gaagattttg cagtgtatta ctgtcaacag ggttatagta gtagtaatct tgataatgtt 300 ttcggcggag ggaccaaggt ggagatcaaa cggaccgtgg ctgcaccatc tgtcttcatc 360 ttcccgccat ctgatgagca gttgaaatct ggaactgcct ctgttgtgtg cctgctgaat 420 aacttctatc ccagagaggc caaagtacag tggaaggtgg ataacgccct ccaatcgggt 480 aactcccagg agagtgtcac agagcaggac agcaaggaca gcacctacag cctcagcagc 540 accctgacgc tgagcaaagc agactacgag aaacacaaag tctacgcctg cgaagtcacc 600 catcagggcc tgagctcgcc cgtcacaaag agcttcaaca ggggagagtg c 651 <![CDATA[<210> 37]]> <![CDATA[<211> 1323]]> <![CDATA[<212> DNA]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> 合成構築體]]> <![CDATA[<400> 37]]> gaggtgcagc tggtggagtc tgggggaggc ttggtccagc ctggagggtc cctgagactc 60 tcctgtgcag cctctggatt cgacatcagt aagtacaaca tccaatgggt ccgccaggct 120 ccagggaagg ggctggagtg ggttggcttc attaattatg gtggtagcgc atactacgcg 180 agccgggcga aaggcagatt caccatctca agagatgatt caaagaactc actgtatctg 240 caaatgaaca gcctgaaaac cgaggacacg gccgtgtatt actgtgctag aggactaagt 300 aatagcgacc tctggggcca gggcaccctg gtcaccgtct cctcagcttc taccaagggc 360 ccatcggtct tcccgctagc gccctgctcc aggagcacct ccgagagcac agccgccctg 420 ggctgcctgg tcaaggacta cttccccgaa ccggtgacgg tgtcgtggaa ctcaggcgcc 480 ctgaccagcg gcgtgcacac cttcccggct gtcctacagt cctcaggact ctactccctc 540 agcagcgtgg tgaccgtgcc ctccagcagc ttgggcacga agacctacac ctgcaacgta 600 gatcacaagc ccagcaacac caaggtggac aagagagttg agtccaaata tggtccccca 660 tgcccaccct gcccagcacc tgaggccgcc gggggaccat cagtcttcct gttcccccca 720 aaacccaagg acactctcat gatctcccgg acccctgagg tcacgtgcgt ggtggtggac 780 gtgagccagg aagaccccga ggtccagttc aactggtacg tggatggcgt ggaggtgcat 840 aatgccaaga caaagccgcg ggaggagcag ttcaacagca cgtaccgtgt ggtcagcgtc 900 ctcaccgtcc tgcaccagga ctggctgaac ggcaaggagt acaagtgcaa ggtctccaac 960 aaaggcctcc cgtcctccat cgagaaaacc atctccaaag ccaaagggca gccccgagag 1020 ccacaggtgt acaccctgcc cccatcccag gaggagatga ccaagaacca ggtcagcctg 1080 acctgcctgg tcaaaggctt ctaccccagc gacatcgccg tggagtggga aagcaatggg 1140 cagccggaga acaactacaa gaccacgcct cccgtgctgg actccgacgg ctccttcttc 1200 ctctacagca ggctaaccgt ggacaagagc aggtggcagg aggggaatgt cttctcatgc 1260 tccgtgatgc atgaggctct gcacaaccac tacacacaga agagcctctc cctgtctctg 1320 ggt 1323 <![CDATA[<210> 38]]> <![CDATA[<211> 663]]> <![CDATA[<212> DNA]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> 合成構築體]]> <![CDATA[<400> 38]]> gacatccaga tgacccagtc tccatcctcc ctgtctgcat ctgtaggaga cagagtcacc 60 atcacttgcc aggccagtca gagcattagt agttggttat cctggtatca gcagaaacca 120 gggaaagccc ctaagctcct gatctacagg gcatccactc tggcatctgg ggtcccatca 180 aggttcagtg gaagtggatc tgggacagat tttactttca ccatcagcag cctgcagcct 240 gaagatattg caacatatta ctgtcaatcc acttatggtg gtgttgttgg cagtactagt 300 gatgataatc ctttcggcgg agggaccaag gtggagatca aacggaccgt ggctgcacca 360 tctgtcttca tcttcccgcc atctgatgag cagttgaaat ctggaactgc ctctgttgtg 420 tgcctgctga ataacttcta tcccagagag gccaaagtac agtggaaggt ggataacgcc 480 ctccaatcgg gtaactccca ggagagtgtc acagagcagg acagcaagga cagcacctac 540 agcctcagca gcaccctgac gctgagcaaa gcagactacg agaaacacaa agtctacgcc 600 tgcgaagtca cccatcaggg cctgagctcg cccgtcacaa agagcttcaa caggggagag 660 tgc 663 <![CDATA[<210> 39]]> <![CDATA[<211> 1341]]> <![CDATA[<212> DNA]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> 合成構築體]]> <![CDATA[<400> 39]]> caggtgcagc tggtgcagtc tggggctgag gtgaagaagc ctggggcctc agtgaaggtt 60 tcctgcaagg catctggatt ctccctcagt acctatgcaa tgaactgggt gcgacaggcc 120 cctggacaag ggcttgagtg gatgggaatc attagtgatg atggtaccac atactacgcg 180 acctgggcga aaggcagagt caccatgacc agggacacgt ccacgagcac agtctacatg 240 gagctgagca gcctgagatc tgaggacacg gccgtgtatt actgtgcgag agatgctggt 300 gctggtggtg tccaagacta cttaaccttg tggggccagg gcaccctggt caccgtctcc 360 tcagcttcta ccaagggccc atcggtcttc ccgctagcgc cctgctccag gagcacctcc 420 gagagcacag ccgccctggg ctgcctggtc aaggactact tccccgaacc ggtgacggtg 480 tcgtggaact caggcgccct gaccagcggc gtgcacacct tcccggctgt cctacagtcc 540 tcaggactct actccctcag cagcgtggtg accgtgccct ccagcagctt gggcacgaag 600 acctacacct gcaacgtaga tcacaagccc agcaacacca aggtggacaa gagagttgag 660 tccaaatatg gtcccccatg cccaccctgc ccagcacctg aggccgccgg gggaccatca 720 gtcttcctgt tccccccaaa acccaaggac actctcatga tctcccggac ccctgaggtc 780 acgtgcgtgg tggtggacgt gagccaggaa gaccccgagg tccagttcaa ctggtacgtg 840 gatggcgtgg aggtgcataa tgccaagaca aagccgcggg aggagcagtt caacagcacg 900 taccgtgtgg tcagcgtcct caccgtcctg caccaggact ggctgaacgg caaggagtac 960 aagtgcaagg tctccaacaa aggcctcccg tcctccatcg agaaaaccat ctccaaagcc 1020 aaagggcagc cccgagagcc acaggtgtac accctgcccc catcccagga ggagatgacc 1080 aagaaccagg tcagcctgac ctgcctggtc aaaggcttct accccagcga catcgccgtg 1140 gagtgggaaa gcaatgggca gccggagaac aactacaaga ccacgcctcc cgtgctggac 1200 tccgacggct ccttcttcct ctacagcagg ctaaccgtgg acaagagcag gtggcaggag 1260 gggaatgtct tctcatgctc cgtgatgcat gaggctctgc acaaccacta cacacagaag 1320 agcctctccc tgtctctggg t 1341 <![CDATA[<210> 40]]> <![CDATA[<211> 651]]> <![CDATA[<212> DNA]]> <![CDATA[<213> 人工序列]]> <![CDATA[<220>]]> <![CDATA[<223> 合成構築體]]> <![CDATA[<400> 40]]> gacatcgtga tgacccagtc tccagactcc ctggctgtgt ctctgggcga gagggccacc 60 atcaactgcc aggccagtga gaatatttac aactttttgg cctggtacca gcagaaacca 120 ggacagcctc ctaagctgct catttactct gcatccactc tggcatctgg ggtccctgac 180 cgattcagtg gcagcgggtc tgggacagat ttcactctca ccatcagcag cctgcaggct 240 gaagatgtgg cagtttatta ctgtcaacag ggttctagta atagtaatat tgataatcct 300 ttcggcggag ggaccaaggt ggagatcaaa cggaccgtgg ctgcaccatc tgtcttcatc 360 ttcccgccat ctgatgagca gttgaaatct ggaactgcct ctgttgtgtg cctgctgaat 420 aacttctatc ccagagaggc caaagtacag tggaaggtgg ataacgccct ccaatcgggt 480 aactcccagg agagtgtcac agagcaggac agcaaggaca gcacctacag cctcagcagc 540 accctgacgc tgagcaaagc agactacgag aaacacaaag tctacgcctg cgaagtcacc 600 catcagggcc tgagctcgcc cgtcacaaag agcttcaaca ggggagagtg c 651 <![CDATA[<210> 41]]> <![CDATA[<211> 283]]> <![CDATA[<212> PRT]]> <![CDATA[<213> 智人]]> <![CDATA[<400> 41]]> Met Glu Pro Pro Gly Asp Trp Gly Pro Pro Pro Trp Arg Ser Thr Pro 1 5 10 15 Lys Thr Asp Val Leu Arg Leu Val Leu Tyr Leu Thr Phe Leu Gly Ala 20 25 30 Pro Cys Tyr Ala Pro Ala Leu Pro Ser Cys Lys Glu Asp Glu Tyr Pro 35 40 45 Val Gly Ser Glu Cys Cys Pro Lys Cys Ser Pro Gly Tyr Arg Val Lys 50 55 60 Glu Ala Cys Gly Glu Leu Thr Gly Thr Val Cys Glu Pro Cys Pro Pro 65 70 75 80 Gly Thr Tyr Ile Ala His Leu Asn Gly Leu Ser Lys Cys Leu Gln Cys 85 90 95 Gln Met Cys Asp Pro Ala Met Gly Leu Arg Ala Ser Arg Asn Cys Ser 100 105 110 Arg Thr Glu Asn Ala Val Cys Gly Cys Ser Pro Gly His Phe Cys Ile 115 120 125 Val Gln Asp Gly Asp His Cys Ala Ala Cys Arg Ala Tyr Ala Thr Ser 130 135 140 Ser Pro Gly Gln Arg Val Gln Lys Gly Gly Thr Glu Ser Gln Asp Thr 145 150 155 160 Leu Cys Gln Asn Cys Pro Pro Gly Thr Phe Ser Pro Asn Gly Thr Leu 165 170 175 Glu Glu Cys Gln His Gln Thr Lys Cys Ser Trp Leu Val Thr Lys Ala 180 185 190 Gly Ala Gly Thr Ser Ser Ser His Trp Val Trp Trp Phe Leu Ser Gly 195 200 205 Ser Leu Val Ile Val Ile Val Cys Ser Thr Val Gly Leu Ile Ile Cys 210 215 220 Val Lys Arg Arg Lys Pro Arg Gly Asp Val Val Lys Val Ile Val Ser 225 230 235 240 Val Gln Arg Lys Arg Gln Glu Ala Glu Gly Glu Ala Thr Val Ile Glu 245 250 255 Ala Leu Gln Ala Pro Pro Asp Val Thr Thr Val Ala Val Glu Glu Thr 260 265 270 Ile Pro Ser Phe Thr Gly Arg Ser Pro Asn His 275 280
Claims (25)
- 一種結合BTLA之抗體,其包含具有SEQ ID NO:15之胺基酸序列的HCDR1、具有SEQ ID NO:18之胺基酸序列的HCDR2、具有SEQ ID NO:21之胺基酸序列的HCDR3、具有SEQ ID NO:24之胺基酸序列的LCDR1、具有SEQ ID NO:27之胺基酸序列的LCDR2以及具有SEQ ID NO:30之胺基酸序列的LCDR3。
- 如請求項1之抗體,其包含具有SEQ ID NO:11之胺基酸序列的重鏈可變區(HCVR)及具有SEQ ID NO:12之胺基酸序列的輕鏈可變區(LCVR)。
- 如請求項1之抗體,其包含具有SEQ ID NO:9之胺基酸序列的重鏈(HC)及具有SEQ ID NO:10之胺基酸序列的輕鏈(LC)。
- 如請求項1之抗體,其包含兩個HC及兩個LC,其中各HC具有SEQ ID NO:9之胺基酸序列,且各輕鏈(LC)具有SEQ ID NO:10之胺基酸序列。
- 如請求項1至4中任一項之抗體,其用於療法中。
- 如請求項1至4中任一項之抗體,其用於治療一或多種風濕性、神經性及皮膚病學疾病。
- 如請求項6之抗體,其中該風濕性疾病為狼瘡性腎炎、全身性紅斑性狼瘡症及類風濕性關節炎中之至少一者。
- 如請求項6之抗體,其中該皮膚病學疾病為異位性皮膚炎及牛皮癬中之至少一者。
- 如請求項6之抗體,其中該神經性疾病為多發性硬化症。
- 一種醫藥組合物,其包含如請求項1至4中任一項之抗體及一或多種醫藥學上可接受之載劑、稀釋劑或賦形劑。
- 一種如請求項1至4中任一項之抗體的用途,其用於製造用於治療風濕性、神經性及皮膚病學疾病中之一或多者的藥劑。
- 如請求項11之抗體之用途,其中該風濕性疾病為狼瘡性腎炎、全身性紅斑性狼瘡症及類風濕性關節炎中之至少一者。
- 如請求項11之抗體之用途,其中該皮膚病學疾病為異位性皮膚炎及牛皮癬中之至少一者。
- 如請求項11之抗體之用途,其中該神經性疾病為多發性硬化症。
- 一種醫藥組合物,其用於治療選自狼瘡性腎炎、全身性紅斑性狼瘡症及類風濕性關節炎中之病況,該醫藥組合物包含有效量之如請求項1至4中任一項之抗體。
- 一種醫藥組合物,其用於治療選自異位性皮膚炎及牛皮癬中之病況,該醫藥組合物包含有效量之如請求項1至4中任一項之抗體。
- 一種醫藥組合物,其用於治療多發性硬化症,該醫藥組合物包含有效量之如請求項1至4中任一項之抗體。
- 一種DNA分子,其包含編碼具有SEQ ID NO:9之胺基酸序列之抗體重鏈的聚核苷酸。
- 一種DNA分子,其包含編碼具有SEQ ID NO:10之胺基酸序列之抗體輕鏈的聚核苷酸。
- 一種DNA分子,其包含編碼具有SEQ ID NO:9之胺基酸序列之抗體重鏈的聚核苷酸序列及編碼具有SEQ ID NO:10之胺基酸序列之抗體輕鏈的聚核苷酸序列。
- 如請求項20之DNA分子,其中編碼該抗體重鏈之該聚核苷酸序列為SEQ ID NO:39,且編碼該抗體輕鏈之該聚核苷酸序列為SEQ ID NO:40。
- 一種哺乳動物細胞,其包含如請求項18之DNA分子及如請求項19之DNA分子,其中該細胞能夠表現包含兩個重鏈及兩個輕鏈之抗體,其中各重鏈具有SEQ ID NO:9之胺基酸序列且各輕鏈具有SEQ ID NO:10之胺基酸序列。
- 一種哺乳動物細胞,其包含如請求項20或21之DNA分子,其中該細胞能夠表現包含兩個重鏈及兩個輕鏈之抗體,其中各重鏈具有SEQ ID NO:9之胺基酸序列且各輕鏈具有SEQ ID NO:10之胺基酸序列。
- 一種用於產生抗體之方法,其中該兩個HC中之每一者之胺基酸序列為SEQ ID NO:9,且該兩個LC中之每一者之胺基酸序列為SEQ ID NO:10,且其中該方法包含:a)在使得該抗體表現之條件下培育如請求項22或23之哺乳動物細胞,及b)回收該經表現抗體。
- 一種抗體,其可藉由如請求項24之方法獲得。
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