Ronchese F, Hausmann B
Basel Institute for Immunology, Switzerland.
J Exp Med. 1993 Mar 1;177(3):679-90. doi: 10.1084/jem.177.3.679.
The ability of B cells or macrophages and dendritic cells (DC) to elicit class II-restricted T cell responses in vivo was compared using a mouse chimera model. Severe combined immunodeficient (SCID) mice (H-2d), reconstituted either with T or T+B lymphocytes from (H-2d x H-2b) donors, were immunized subcutaneously with protein antigen (Ag) to induce a class II-restricted T cell response. The frequency and major histocompatibility complex restriction of the resulting Ag-specific T cells were analyzed to establish whether B cells were necessary for the induction of class II-restricted T cell responses, and to determine the cell type on which priming had occurred. The results indicated that: (a) B cells are not necessary for the induction of a class II-restricted T cell response in vivo, as the frequencies of interleukin 2 (IL-2)- or IL-3-secreting T cells induced in the presence or absence of B cells were comparable. (b) Activation of naive T cells requires presentation of Ag on DC; Ag presented only on B cells is not sufficient to elicit a response. No H-2b-restricted, IL-3-secreting cells could in fact be detected in SCID mice reconstituted with naive (H-2d x H-2b) T cells and nonimmune or antigen-primed (H-2d x H-2b) B cells. (c) Previously primed T cells are able to be stimulated by Ag presented by both B cells and DC. H-2b-restricted, IL-3-secreting cells could in fact be readily demonstrated in SCID mice reconstituted with antigen-primed (H-2d x H-2b) T and B cells. Irrespective of whether the T cells were naive or previously activated, B cells were able to respond with an Ag-specific immunoglobulin G response, indicating that B cells were functional and able to present Ag in order to receive specific T cell help. Therefore, it appears that B cells are not necessary and do not participate in the initial priming of T cells; however, Ag presented by B cells can reactivate previously primed T cells. Taken together, these data indicate that during the course of an immune response Ag is first presented to naive T cells via DC, and only subsequently primed T cells can be stimulated by Ag presented by B cells.
利用小鼠嵌合体模型比较了B细胞、巨噬细胞和树突状细胞(DC)在体内引发II类限制性T细胞反应的能力。用来自(H-2d×H-2b)供体的T或T + B淋巴细胞重建的严重联合免疫缺陷(SCID)小鼠(H-2d),皮下注射蛋白质抗原(Ag)以诱导II类限制性T细胞反应。分析所得Ag特异性T细胞的频率和主要组织相容性复合体限制性,以确定B细胞对于诱导II类限制性T细胞反应是否必要,并确定引发反应的细胞类型。结果表明:(a)B细胞对于体内诱导II类限制性T细胞反应不是必需的,因为在有或没有B细胞存在的情况下诱导的分泌白细胞介素2(IL-2)或IL-3的T细胞频率相当。(b)幼稚T细胞的激活需要DC上Ag的呈递;仅在B细胞上呈递的Ag不足以引发反应。在用幼稚(H-2d×H-2b)T细胞和非免疫或抗原致敏(H-2d×H-2b)B细胞重建的SCID小鼠中,实际上未检测到H-2b限制性、分泌IL-3的细胞。(c)先前致敏的T细胞能够被B细胞和DC呈递的Ag刺激。在用抗原致敏的(H-2d×H-2b)T和B细胞重建的SCID小鼠中,实际上很容易证明存在H-2b限制性、分泌IL-3的细胞。无论T细胞是幼稚的还是先前已激活的,B细胞都能够以Ag特异性免疫球蛋白G反应作出应答,表明B细胞具有功能并且能够呈递Ag以接受特异性T细胞的辅助。因此,似乎B细胞不是必需的,并且不参与T细胞的初始致敏;然而,B细胞呈递的Ag可以重新激活先前致敏的T细胞。总之,这些数据表明在免疫反应过程中,Ag首先通过DC呈递给幼稚T细胞,只有随后致敏的T细胞才能被B细胞呈递的Ag刺激。