Crispe I N, Gascoigne N R, Owens T
Immunology. 1984 May;52(1):55-65.
Both B lymphocytes and cytotoxic T lymphocytes respond to signals from the T helper (Th) compartment, and such signals are mediated by a number of biochemically distinct factors. This raises the question whether help for B cells and T cells is a function of one or several different kinds of Th cell. Here we describe an in vitro and in vivo study of this problem, using a Th clone, designated MTH-1. The clone carries the cell surface markers Thy-1 and L3T4a, but lacks Lyt-2. It recognizes a minor alloantigen shared by DBA/2, B10.D2 and NZB spleen cells, and such recognition is restricted by H-2Ed. Recognition of antigen in vitro is accompanied by secretion of IL-2. In vivo, both primary and secondary CTL responses to multiple minor alloantigens are enhanced by small numbers (less than or equal to 10(4] of MTH-1 cells. Recognition of alloantigen in a T-depleted B cell population results in the polyclonal activation and maturation of the B cells to secrete immunoglobulin; also, antigen-primed B cells are augmented in their in vivo synthesis of specific antibody to the Thy-1 X 1 alloantigen by around 10(5) MTH-1 cells. Taken together, these results suggest a single Th clone can help both B cells and T cells.
B淋巴细胞和细胞毒性T淋巴细胞都对来自辅助性T细胞(Th)区室的信号作出反应,并且这些信号由多种生物化学性质不同的因子介导。这就提出了一个问题,即对B细胞和T细胞的辅助是由一种还是几种不同类型的Th细胞发挥作用。在此,我们使用一个名为MTH-1的Th克隆对这个问题进行了体外和体内研究。该克隆携带细胞表面标志物Thy-1和L3T4a,但缺乏Lyt-2。它识别由DBA/2、B10.D2和NZB脾细胞共享的一种次要同种异体抗原,并且这种识别受H-2Ed限制。体外对抗原的识别伴随着白细胞介素-2的分泌。在体内,少量(小于或等于10⁴)的MTH-1细胞可增强对多种次要同种异体抗原的初次和二次细胞毒性T淋巴细胞反应。在T细胞缺失的B细胞群体中对同种异体抗原的识别导致B细胞多克隆活化和成熟以分泌免疫球蛋白;此外,经抗原致敏的B细胞在体内针对Thy-1×1同种异体抗原的特异性抗体合成可被约10⁵个MTH-1细胞增强。综上所述,这些结果表明单个Th克隆可以同时辅助B细胞和T细胞。