Petro T M, Chen S S, Panther R B
Dept. of Oral Biology, University of Nebraska Medical Center, Lincoln, USA.
Immunol Invest. 1995 Nov;24(6):965-76. doi: 10.3109/08820139509060721.
Conjugation of the T cell receptor (TCR) with antigen/MHC proteins must be accompanied by conjugation of T cell counterreceptors (CD28 or CTLA-4) with costimulatory molecules CD80 or CD86 (B7-1 or B7-2) on antigen presenting cells (APC) to avert T cell anergy, and to provide essential signals for T cell activation and cytokine production. However, T cells and APC express changing patterns of counterreceptors and costimulatory molecules during the immune response. To determine the involvement of CD80 and CD86 in costimulation of T cell cytokine production, T cells were incubated with peritoneal exudate macrophages, which express CD80 and CD86, and stimulated in vitro for 48 or 72 hrs with anti-CD3 in the presence or absence of blocking antibody to CD80 or CD86. Alternatively, enriched anti-CD3 stimulated T cells were costimulated with antibody to CD28 and CTLA-4. Production of T cell IL-2, IL-4, and IL-5 was depressed in the presence of anti-CD86 but not anti-CD80. Production of IFN-gamma was significantly blocked by either anti-CD80 and anti-CD86. Anti-CD28 was a potent costimulator of IFN-gamma and IL-2 production, but a less potent costimulator of IL-4 and IL-5 production. The data suggest that T cell counterreceptors and APC costimulatory molecules act with varying efficacies at stimulating production of T cell cytokines.
T细胞受体(TCR)与抗原/MHC蛋白的结合必须伴随着T细胞共受体(CD28或CTLA-4)与抗原呈递细胞(APC)上的共刺激分子CD80或CD86(B7-1或B7-2)的结合,以避免T细胞无反应性,并为T细胞活化和细胞因子产生提供必要信号。然而,在免疫反应过程中,T细胞和APC表达的共受体和共刺激分子模式会发生变化。为了确定CD80和CD86在T细胞细胞因子产生的共刺激中的作用,将T细胞与表达CD80和CD86的腹腔渗出巨噬细胞一起孵育,并在存在或不存在抗CD80或抗CD86阻断抗体的情况下,用抗CD3体外刺激48或72小时。或者,用抗CD28和CTLA-4抗体对富集的抗CD3刺激的T细胞进行共刺激。在存在抗CD86但不存在抗CD80的情况下,T细胞IL-2、IL-4和IL-5的产生受到抑制。IFN-γ的产生被抗CD80和抗CD86显著阻断。抗CD28是IFN-γ和IL-2产生的有效共刺激剂,但对IL-4和IL-5产生的共刺激作用较弱。数据表明,T细胞共受体和APC共刺激分子在刺激T细胞细胞因子产生时具有不同的效力。