Spear G T, Sullivan B L, Landay A L, Lint T F
Department of Immunology/Microbiology, Rush-Presbyterian-St. Luke's Medical Center, Chicago, Illinois 60612.
J Virol. 1990 Dec;64(12):5869-73. doi: 10.1128/JVI.64.12.5869-5873.1990.
The ability of complement to inactivate human immunodeficiency virus (HIV) in the presence of specific antibody was evaluated. HIV was treated with complement and/or antibody, and then its titer was determined on the CD4+ H9 cell line. While complement alone had no effect on the HIV titer, complement plus subneutralizing levels of antibody resulted in titer reductions. Complement sources deficient in membrane attack component C5 or C8 did not inactivate antibody-treated HIV, suggesting that neutralization occurred via lysis. This possibility was investigated by assessing release of reverse transcriptase (RT) from the virion. Antibody plus complement, but neither reagent alone, released RT from HIV in a dose-dependent manner. Release of RT did not occur with C5- or C8-deficient sera, also indicating a requirement for membrane attack components. These studies show that complement can neutralize HIV via the classical complement pathway and that this neutralization occurs via C5b-9-mediated viral lysis. Thus, complement may play a major role in resistance to disease by lysing HIV and preventing infection of Fc- and complement receptor-positive cells, as well as CD4+ cells.
评估了补体在特异性抗体存在下使人类免疫缺陷病毒(HIV)失活的能力。用补体和/或抗体处理HIV,然后在CD4 + H9细胞系上测定其滴度。单独的补体对HIV滴度没有影响,但补体加上亚中和水平的抗体导致滴度降低。缺乏膜攻击成分C5或C8的补体来源不能使经抗体处理的HIV失活,这表明中和作用是通过裂解发生的。通过评估逆转录酶(RT)从病毒颗粒中的释放来研究这种可能性。抗体加补体,但单独使用任何一种试剂都不能以剂量依赖的方式从HIV中释放RT。缺乏C5或C8的血清不会发生RT释放,这也表明需要膜攻击成分。这些研究表明,补体可以通过经典补体途径中和HIV,并且这种中和作用是通过C5b-9介导的病毒裂解发生的。因此,补体可能通过裂解HIV并防止Fc和补体受体阳性细胞以及CD4 +细胞感染而在疾病抵抗中发挥主要作用。