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由体外免疫的未致敏供体细胞转移的过继性免疫。

Adoptive immunity transferred by naive donor cells immunized in vitro.

作者信息

Adler F L, Adler L T, Seferian P G, Rodkey L S

机构信息

Division of Immunology, St Jude Children's Research Hospital, Memphis.

出版信息

Bone Marrow Transplant. 1989 Nov;4(6):663-8.

PMID:2819284
Abstract

Speedy restoration of immune responsiveness in bone marrow recipients has been the objective of studies in which the donor was immunized so that specific immunologic memory could be transferred adoptively and selectively. Using unrelated rabbits, matched for major histocompatibility antigens but mismatched for their immunoglobulin allotypes, it could be shown that recipients of lymphoid cells from naive donors became B cell chimeras but did not use donor-derived B cells for their antibody responses to test antigens. In contrast, cells from donors primed for such antigens dominated antibody production in recipients in response to specific challenge. Clonal restriction in such adoptive responses was demonstrated. We now show that the induction of effective memory in cells from naive donors can be achieved in vitro during the preparation of donor cells for transfer to the recipient. Early challenge of the recipient enhances expression of the transferred immune response quantitatively and also results in the establishment or preservation of a larger diversity of clones from the donor.

摘要

骨髓移植受者免疫反应的快速恢复一直是相关研究的目标,这些研究中供体接受免疫,以便特异性免疫记忆能够被过继性且选择性地转移。使用主要组织相容性抗原匹配但免疫球蛋白同种异型不匹配的无关兔子,结果显示来自未致敏供体的淋巴细胞受体成为B细胞嵌合体,但在针对测试抗原的抗体反应中并未使用供体来源的B细胞。相反,针对此类抗原致敏的供体细胞主导了受体针对特异性攻击的抗体产生。证实了此类过继性反应中的克隆限制。我们现在表明,在将供体细胞制备用于转移给受体的过程中,可在体外实现未致敏供体细胞中有效记忆的诱导。对受体的早期攻击在数量上增强了转移免疫反应的表达,并且还导致供体来源的更大克隆多样性的建立或保留。

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