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HIV-1特异性B细胞活化。HIV-1感染期间自发B细胞活化的主要成分。

HIV-1-specific B cell activation. A major constituent of spontaneous B cell activation during HIV-1 infection.

作者信息

Amadori A, Zamarchi R, Ciminale V, Del Mistro A, Siervo S, Alberti A, Colombatti M, Chieco-Bianchi L

机构信息

Institute of Oncology, University of Padova, Italy.

出版信息

J Immunol. 1989 Oct 1;143(7):2146-52.

PMID:2476498
Abstract

B cell activation is a well known consequence of HIV-1 infection, and seropositive subjects show high numbers of spontaneously activated Ig-secreting cells in circulation. To better define the importance of the HIV-1-specific response in this phenomenon, we first studied whether in vitro spontaneous anti-HIV-1 antibody production was accompanied by reactivation of memory B lymphocytes. Unstimulated PBL from HIV-1-infected individuals with prior history of hepatitis B and/or EBV infection did not consistently show spontaneous in vitro synthesis of anti-hepatitis B core Ag or anti-EBV antibodies; in addition, PWM-induced synthesis of anti-hepatitis B virus and anti-EBV antibodies was decreased compared to HIV-1-seronegative subjects. Moreover, in comparing the frequencies of activated HIV-1-specific B cell precursors and activated Ig-secreting precursors in limiting dilution experiments, a sizable fraction (20 to 40%) of circulating cells spontaneously secreting Ig produced antibody against HIV-1 determinants. The ratio between the two frequencies fitted in very well with the amount of Ig removed from unstimulated culture supernatants after HIV-1-specific antibody absorption with solid-phase HIV-1. These findings indicate that B cell activation during HIV-1 infection is mainly oriented toward a specific response to HIV-1 determinants; the possible relevance of this phenomenon to lymphomagenesis in AIDS patients is discussed.

摘要

B细胞活化是HIV-1感染的一个众所周知的后果,血清反应阳性的受试者循环中显示出大量自发活化的分泌Ig的细胞。为了更好地确定HIV-1特异性反应在这一现象中的重要性,我们首先研究了体外自发产生抗HIV-1抗体是否伴随着记忆B淋巴细胞的重新激活。来自有乙肝和/或EBV感染既往史的HIV-1感染者的未刺激外周血淋巴细胞(PBL)并未始终显示出体外自发合成抗乙肝核心抗原或抗EBV抗体;此外,与HIV-1血清阴性受试者相比,PWM诱导的抗乙肝病毒和抗EBV抗体的合成减少。此外,在有限稀释实验中比较活化的HIV-1特异性B细胞前体和活化的分泌Ig前体的频率时发现,相当一部分(20%至40%)循环中自发分泌Ig的细胞产生了针对HIV-1决定簇的抗体。这两个频率之间的比率与用固相HIV-1进行HIV-1特异性抗体吸收后从未刺激培养上清液中去除的Ig量非常吻合。这些发现表明,HIV-1感染期间的B细胞活化主要针对对HIV-1决定簇的特异性反应;讨论了这一现象与艾滋病患者淋巴瘤发生的可能相关性。

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