Thomson A W, Bonham C A
Pittsburgh Transplantation Institute, University of Pittsburgh Medical Center, Pennsylvania 15213, USA.
Adv Exp Med Biol. 1995;374:211-6. doi: 10.1007/978-1-4615-1995-9_18.
Theoretically, drugs that inhibit programmed cell death could be used to inhibit the increased apoptotic decay of lymphocyte populations in human immunodeficiency virus (HIV) infection. The concept that immunopathologic processes cause immune suppression provides a further rationale for the use of agents such as cyclosporin A (CsA) or tacrolimus (formerly known as FK506) early in HIV infection to reduce cytotoxic CD8+ T cell-mediated destruction of HIV-infected target cells.
从理论上讲,抑制程序性细胞死亡的药物可用于抑制人类免疫缺陷病毒(HIV)感染中淋巴细胞群体凋亡增加的情况。免疫病理过程导致免疫抑制这一概念为在HIV感染早期使用环孢素A(CsA)或他克莫司(原称FK506)等药物提供了进一步的理论依据,以减少细胞毒性CD8 + T细胞介导的HIV感染靶细胞的破坏。