JP2018522001A - ヒト及び/又は動物における免疫応答を調節及び/又は刺激するための組成物及び方法 - Google Patents
ヒト及び/又は動物における免疫応答を調節及び/又は刺激するための組成物及び方法 Download PDFInfo
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Abstract
Description
C型レクチン受容体デクチン1は、サッカロマイセス・セレビシエ由来のベータ―グルカンと結合し、特に食作用及びザイモサン、サッカロマイセス・セレビシエ由来の細胞壁抽出物等の粒子やサッカロマイセス・セレビシエ系統由来の他の酵母誘導体(他の酵母誘導体は限定されないが、酵母細胞壁、不活性酵母又は自己消化酵母)の除去を導く様々な経路の誘導に関与することが記載されている(Marakalaら、Mamm Genome (2011) 22:55−65)。脅威を検出する機構及び感染に対する迅速な応答は高度に保存されており、免疫応答はこの病原体リガンドの、例えばベータ―グルカンの、宿主細胞の表面上のPRRへの結合によって部分的に引き起こされる。炎症に関連して、数時間以内に、非特異的自然免疫系が活性化される。局所炎症は、感染に対するこの迅速な応答に重要な役割を果たしている。自然免疫系における多くのプレーヤーは、好中球、単球、マクロファージ、補体因子、サイトカイン、抗微生物ペプチド及び急性期タンパク質を含めて、複雑で非常に調節された応答で素早く起動して、感染に対して迅速に防御する。最近では、前記経路を通じた免疫応答の刺激を謳った非特異的で不活性な酵母を基礎とする製品に対する市場選択肢が存在している。しかしながら、これらの製品は特異性及び成果の点で一貫性に欠いている。動物又はヒトの免疫応答の刺激を増強する改善された酵母製品を提供することは非常に望ましいことである。
サッカロマイセス・セレビシエ菌株:L60、L62、L69、L72
カンジダ・ユチリス菌株:L75(NRRL−900)
様々なアッセイで試験した菌体壁多糖のレベル:
カンジダ・ユチリス菌株:菌体壁多糖レベルは、組成物の総重量を基準として30乾燥重量%に標準化した。
サッカロマイセス・セレビシエ菌株:菌体壁多糖レベルは、組成物の総重量を基準として30、35、45、及び60乾燥重量%に標準化した。
カンジダ・ユチリス及びサッカロマイセス・セレビシエの組み合わせ:多糖レベルは、組成物の総重量を基準として30、35、45、及び50乾燥重量%に標準化した。これら組み合わせ中のカンジダ・ユチリスに由来する菌体壁多糖のレベルは、それぞれ、組成物の総重量を基準として15、15、10、15、及び5乾燥重量%、又は組成物中の菌体壁多糖の総重量を基準として50、43、25、33、及び10乾燥重量%だった(図4a及び4b)。
・カンジダ・ユチリスNRRL−900に由来する菌体壁多糖を6乾燥重量%(組成物の総重量を基準として、又は組成物中の菌体壁多糖の総重量を基準として12乾燥重量%)含有する50SC/CU菌体壁多糖:3用量を試験した:飼料中0.04%、0.08%、0.12%。
・S.セレビシエの1つの菌株(CNCM I 1079)に由来する60SC菌体壁多糖を、飼料中0.12%で試験した。
・T−1:対照−酵母誘導体を含まない通常食餌
・T−2:0.08%の50SC/CU菌体壁多糖で補完された対照食餌
・各飼養段階の開始時及び終了時の1檻当たりの体重、
・第2飼養段階の1檻当たりの飼料消費量
・死亡率及び淘汰率
・動物の総数:開始時129匹、終了時125匹。
・性別:雄
・血統:フリージアン(由来:フランスの異なる農場)
T0として:製品を一切含まない対照食餌。
T1:50SC/CU菌体壁多糖で補完した同じ食餌
・最初の2週間:5g/動物/日=2.7g/kgの開始飼料
・その後:3g/動物/日=1.6g/kgの開始飼料
・到着日〜2週間:2×1.5L/日の初乳ミルク希釈液(25%CP及び19.5%脂肪)、その後代用ミルク(22%CP及び18%脂肪)+固形飼料(粉末ミール)自由摂取+ストロー自由摂取+水自由摂取。
・2週間〜離乳(34日):1×2L/日の代用ミルク(19%CP及び15%脂肪)+固形飼料(粉末ミール)自由摂取+ストロー自由摂取+水自由摂取。
・離乳〜出荷:固形飼料(粉末ミール)自由摂取+ストロー自由摂取+水自由摂取
・体重:個々、実験の開始時及び終了時及び食餌変更時。
・飼料摂取量:1檻当たり。食餌変更時に、供給した飼料と変更した日に残っていた飼料の差として。
・罹患率:定期的な集団単位の予防を含む、個体及び集団単位の医療行為。
・死亡率:日付、体重、及び考えられる理由。
・下痢:1檻当たり。下痢発生の日常的点検。
Yjk=μ+axIBW+バッチj+処置k+バッチj*処置k+ejk
・離乳後の食餌に50SC/CU PARIETAL POLYSACCHARIDESを添加することにより、限定的な薬物処方を伴う対照食餌と比べて、最終体重、全体の平均1日増体量、及び全体飼料要求率が数値的な向上する。
・この影響は、恐らくは農場での健康状態に応じて、プレ開始期間よりも開始期間でより大きいと思われる。
・50SC/CU PARIETAL POLYSACCHARIDESは、開始段階中のZnO及び/又は抗生物質の良好で有望な代用物である可能性がある。
50SC/CU PARIETAL POLYSACCHARIDES処置を陽性対照と比較して、50SC/CU PARIETAL POLYSACCHARIDESが抗生物質の代わりになる可能性を試験すること、及び抗生物質に加えて50SC/CU PARIETAL POLYSACCHARIDESを添加することが及ぼす補完的効果の可能性を試験することが推奨される。
・D14:コクシジウム症負荷=それぞれ75,000、25,000、及び50,000のE.アセルブリナ、E.マキシマ、及びE.テネラ
・D20:糞便物(ケージ毎に混合)中の接合子嚢数(oocysts count)
腸病変スコアリング(5羽の鳥/ケージ)
結果
Claims (25)
- 少なくとも1種のカンジダ種からの菌体壁多糖及び少なくとも1種の異なる酵母種からの菌体壁多糖を含む組成物。
- 前記少なくとも1種のカンジダ種からの菌体壁多糖の量が、前記組成物中の菌体壁多糖の総重量を基準として10〜50乾燥重量%である、請求項1に記載の組成物。
- 前記少なくとも1種のカンジダ種からの菌体壁多糖の量が、前記組成物中の菌体壁多糖の総重量を基準として10〜15乾燥重量%である、請求項1又は2に記載の組成物。
- 前記少なくとも1種のカンジダ種からの菌体壁多糖の量が、前記組成物中の菌体壁多糖の総重量を基準として少なくとも10、15、20、25、30、35、40、45又は50乾燥重量%である、請求項2に記載の組成物。
- 前記少なくとも1種のカンジダ種からの菌体壁多糖の量が、前記組成物中の菌体壁多糖の総重量を基準として少なくとも10、11、12、13、14又は15乾燥重量%である、請求項3に記載の組成物。
- 前記少なくとも1種のカンジダ種からの菌体壁多糖及び前記少なくとも1種の異なる酵母種からの菌体壁多糖の量が、前記組成物の総重量を基準として20〜80重量%である、請求項1〜5のいずれか1項に記載の組成物。
- 前記少なくとも1種のカンジダ種からの菌体壁多糖及び前記少なくとも1種の異なる酵母種からの菌体壁多糖の量が、前記組成物の総重量を基準として30〜60重量%である、請求項1〜6のいずれか1項に記載の組成物。
- 前記少なくとも1種のカンジダ種からの菌体壁多糖及び前記少なくとも1種の異なる酵母種からの菌体壁多糖の量が、前記組成物の総重量を基準として少なくとも20、23、25、27、30、33、35、37、40、43、45、47、50、53、55、57、60、63、65、67、70、73、75、77又は80重量%である、請求項1〜5のいずれか1項に記載の組成物。
- 前記少なくとも1種のカンジダ種からの菌体壁多糖及び前記少なくとも1種の異なる酵母種からの菌体壁多糖の量が、前記組成物の総重量を基準として少なくとも30、31、32、33、34、35、36、37、38、39、40、41、42、43、44、45、46、47、48、49、50、51、52、53、54、55、56、57、58、59又は60重量%である、請求項1〜5のいずれか1項に記載の組成物。
- 前記少なくとも1種のカンジダ種からの菌体壁多糖の量が、前記組成物中の菌体壁多糖の総重量を基準として10〜50乾燥重量%であり、かつ、前記少なくとも1種のカンジダ種からの菌体壁多糖及び前記少なくとも1種の異なる酵母種からの菌体壁多糖の量が、前記組成物の総重量を基準として30〜60重量%である、請求項1に記載の組成物。
- 前記少なくとも1種のカンジダ種からの菌体壁多糖の量が、前記組成物中の菌体壁多糖の総重量を基準として少なくとも10、15、20、25、30、35、40、45又は50乾燥重量%であり、かつ、前記少なくとも1種のカンジダ種からの菌体壁多糖及び前記少なくとも1種の異なる酵母種からの菌体壁多糖の量が、前記組成物の総重量を基準として30〜60重量%である、請求項1に記載の組成物。
- 前記少なくとも1種のカンジダ種からの菌体壁多糖の量が、前記組成物中の菌体壁多糖の総重量を基準として10〜50乾燥重量%であり、かつ、前記少なくとも1種のカンジダ種からの菌体壁多糖及び前記少なくとも1種の異なる酵母種からの菌体壁多糖の量が、前記組成物の総重量を基準として少なくとも30、31、32、33、34、35、36、37、38、39、40、41、42、43、44、45、46、47、48、49、50、51、52、53、54、55、56、57、58、59又は60重量%である、請求項1に記載の組成物。
- 前記少なくとも1種のカンジダ種からの菌体壁多糖の量が、前記組成物中の菌体壁多糖の総重量を基準として少なくとも10、15、20、25、30、35、40、45又は50乾燥重量%であり、かつ、前記少なくとも1種のカンジダ種からの菌体壁多糖及び前記少なくとも1種の異なる酵母種からの菌体壁多糖の量が、前記組成物の総重量を基準として少なくとも30、31、32、33、34、35、36、37、38、39、40、41、42、43、44、45、46、47、48、49、50、51、52、53、54、55、56、57、58、59又は60重量%である、請求項1に記載の組成物。
- 前記少なくとも1種のカンジダ種がカンジダ・ユチリスである、請求項1〜13のいずれか1項に記載の組成物。
- 前記少なくとも1種の異なる酵母種からの菌体壁多糖が、サッカロマイセス種、ハンセニアスポラ種、ハンゼヌラ種、クルイベロマイセス種、メチニコビア種、ピキア種、スターメレラ種及びトルラスポラ種又はこれらの混合種由来である、請求項1〜14のいずれか1項に記載の組成物。
- 動物において免疫応答を調節及び/又は刺激するのに使用するための、請求項1〜15のいずれか1項に記載の組成物。
- 動物の腸管の健康、腸管の完全性及び腸管の形態を改善するのに使用するための、請求項1〜15のいずれか1項に記載の組成物。
- 動物の抗炎症応答を刺激するのに使用するための、請求項1〜15のいずれか1項に記載の組成物。
- 飼育動物の成長成績パラメータ及び飼料要求率を改善するのに使用するための、請求項1〜15のいずれか1項に記載の組成物。
- 飼育動物の罹患率、特には抗生物質による治療及び死亡率を低減するのに使用するための、請求項1〜15のいずれか1項に記載の組成物。
- 飼育動物の死亡率を低下させるのに使用するための、請求項1〜15のいずれか1項に記載の組成物。
- 動物の下痢を減少させるのに使用するための、請求項1〜15のいずれか1項に記載の組成物。
- 腸管病原体に対する感受性を低下させるのに使用するための、請求項1〜15のいずれか1項に記載の組成物。
- 寄生虫侵襲及び関連疾患に対する動物の感受性を低下させるのに使用するための、請求項1〜15のいずれか1項に記載の組成物。
- 水生動物の皮膚粘液の産生を改善するのに使用するための、請求項1〜15のいずれか1項に記載の組成物。
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JP2021183608A (ja) | 2021-12-02 |
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JP7252758B2 (ja) | 2023-04-05 |
ES2953462T3 (es) | 2023-11-13 |
BR112018000102A2 (pt) | 2018-09-04 |
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