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Modulation of the in vivo primate anti-Gal response through administration of anti-idiotypic antibodies.

作者信息

McMorrow Isabel M, Buhler Leo, Treter Sarah, Neethling Francisca A, Alwayn Ian P J, Comrack Christopher A, Kitamura Hiroshi, Awwad Michel, DerSimonian Harout, Cooper David K C, Sachs David H, LeGuern Christian

机构信息

Transplantation Biology Research Center, Massachusetts General Hospital/Harvard Medical School, Boston 02129, USA.

出版信息

Xenotransplantation. 2002 Mar;9(2):106-14. doi: 10.1034/j.1399-3089.2002.1o028.x.

Abstract

Polyclonal anti-idiotypic antibodies (AIA) were generated against human Gal alpha 1,3Gal antibodies (anti-Gal) isolated from a single donor. Specificity of the AIA was demonstrated by selective binding to anti-Gal antibodies (Ab) and absence of reactivity to non-Gal Ab. The idiotopes identified by AIA were present on anti-Gal Ab from all of the human samples evaluated (n=59) as well as on pooled samples, demonstrating that a restricted number of dominant idiotopes characterized the human anti-Gal Ab response. Furthermore, the AIA had cross-species reactivity with baboon serum samples (n=19), suggesting that the overall shape of the anti-Gal Ab combining site is conserved throughout the Old World primates and providing additional evidence of the limited heterogeneity of the anti-Gal Ab repertoire. In order to evaluate the potential effect of AIA in the modulation of the anti-Gal response in vivo, a baboon was injected with repeated doses of the purified AIA. Following AIA treatment, new Ab were generated that reduced Ab-mediated cytotoxicity to porcine cells. Furthermore, administration of the AIA to a baboon prolonged the survival of intravenously infused pig hematopoietic cells when compared with their survival in a control baboon that did not receive prior AIA treatment but underwent a similar conditioning regimen.

摘要

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