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来自HIV血清阳性个体的B细胞的HIV诱导的、HIV特异性体外抗体应答。

HIV-induced, HIV-specific in vitro antibody response by B-cells from HIV-seropositive individuals.

作者信息

Delfraissy J F, Wallon C, Boué F, Goujard C, Barré-Sinoussi F, Galanaud P

机构信息

INSERM U131, Clamart, France.

出版信息

AIDS. 1992 Jan;6(1):55-63. doi: 10.1097/00002030-199201000-00007.

Abstract

OBJECTIVE

Recent studies have shown that B-cells from HIV-infected patients can secrete anti-HIV antibodies in vitro and that they represent 20-40% of immunoglobulin (Ig)-secreting B-cells in vivo. This study was designed to investigate the precise role of HIV in this in vitro antibody production.

DESIGN AND METHODS

B-cells from HIV-infected patients [asymptomatic, n = 28; symptomatic (AIDS), n = 14], from seronegative adult volunteers (n = 22) and subjects at high risk for HIV infection (n = 15) were cultured in vitro in the presence of pokeweed mitogen, Staphylococcus aureus cowan or HIV, and T-cells or interleukins (IL). Non-specific Ig production and specific anti-HIV antibody (Ab) production were measured by enzyme-linked immunosorbent and Western blot assays.

RESULTS

We found that HIV induced a specific response in cultured B-cells from seropositive patients, in contrast with cultured B-cells from uninfected normal individuals. The characteristics of the HIV-induced response differed from those of a spontaneous or a mitogen-induced response. Anti-HIV Ab production was optimal on day 8-10, when B-cells were cultured with recombinant IL-2 and recombinant interferon-alpha in the presence of infectious virus or recombinant gp160 Env protein. The anti-HIV Ab were mainly directed against Env proteins. Interaction of HIV with B-cells involved surface IgG but not CD4 antigen. Autologous CD8+ T-cells had a non-specific inhibitory effect. Both CD5+ and CD5- B-cells produced anti-HIV Ab. No anti-HIV Ab production was observed in B-cells from high-risk HIV-seronegative individuals.

CONCLUSION

HIV (infectious virus or gp160) can induce B-cells from infected patients to secrete specific anti-HIV Ab in vitro.

摘要

目的

近期研究表明,来自HIV感染患者的B细胞在体外可分泌抗HIV抗体,且在体内它们占分泌免疫球蛋白(Ig)的B细胞的20%-40%。本研究旨在调查HIV在这种体外抗体产生过程中的精确作用。

设计与方法

将来自HIV感染患者[无症状者,n = 28;有症状者(艾滋病患者),n = 14]、血清学阴性的成年志愿者(n = 22)以及HIV感染高危人群(n = 15)的B细胞,在体外与商陆有丝分裂原、金黄色葡萄球菌考恩株或HIV,以及T细胞或白细胞介素(IL)一起培养。通过酶联免疫吸附测定法和蛋白质印迹法检测非特异性Ig产生及特异性抗HIV抗体(Ab)产生情况。

结果

我们发现,与未感染的正常个体培养的B细胞相比,HIV可诱导血清学阳性患者培养的B细胞产生特异性反应。HIV诱导的反应特征不同于自发反应或有丝分裂原诱导的反应。当B细胞在感染性病毒或重组gp160 Env蛋白存在的情况下与重组IL-2和重组干扰素-α一起培养时,抗HIV Ab产生在第8至10天达到最佳。抗HIV Ab主要针对Env蛋白。HIV与B细胞的相互作用涉及表面IgG而非CD4抗原。自体CD8 + T细胞具有非特异性抑制作用。CD5 +和CD5 - B细胞均产生抗HIV Ab。在HIV血清学阴性的高危个体的B细胞中未观察到抗HIV Ab产生。

结论

HIV(感染性病毒或gp160)可在体外诱导感染患者的B细胞分泌特异性抗HIV Ab。

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