Yammani Rama D, Leyva Marcela A, Jennings Ryan N, Haas Karen M
Department of Microbiology and Immunology, Wake Forest School of Medicine, Winston-Salem, NC 27101.
Department of Microbiology and Immunology, Wake Forest School of Medicine, Winston-Salem, NC 27101
J Immunol. 2014 Dec 1;193(11):5434-43. doi: 10.4049/jimmunol.1401462. Epub 2014 Oct 22.
Reductions in C4 levels may predispose individuals to infection with encapsulated bacteria as well as autoimmunity. In this study, we examined the role C4 has in protection against Streptococcus pneumoniae-induced autoimmunity. Mild respiratory infection with serotype 19F pneumococci selectively induced systemic anti-dsDNA IgA production in naive C4(-/-) mice, but not in C3(-/-) or wild-type mice. Systemic challenge with virulent serotype 3 pneumococci also induced anti-dsDNA IgA production in immune C4(-/-) mice. Remarkably, pneumococcal polysaccharide (PPS) vaccination alone induced C4(-/-) mice to produce increased anti-dsDNA IgA levels that were maintained in some mice for months. These effects were most pronounced in female C4(-/-) mice. Importantly, immunization-induced increases in anti-dsDNA IgA levels were strongly associated with increased IgA deposition in kidneys. Cross-reactivity between pneumococcal Ags and dsDNA played a partial role in the induction of anti-dsDNA IgA, but a major role for PPS-associated TLR2 agonists was also revealed. Administration of the TLR2/4 antagonist, OxPAPC, at the time of PPS immunization completely blocked the production of anti-dsDNA IgA in C4(-/-) mice without suppressing PPS-specific Ab production. The TLR2 agonist, Pam3CSK4, similarly induced anti-dsDNA IgA production in C4(-/-) mice, which OxPAPC also prevented. LPS, a TLR4 agonist, had no effect. Pam3CSK4, but not LPS, also induced dsDNA-specific IgA production by C4(-/-) splenic IgA(+) B cells in vitro, indicating that TLR2 agonists can stimulate autoantibody production via B cell-intrinsic mechanisms. Collectively, our results show an important role for C4 in suppressing autoantibody production elicited by cross-reactive Ags and TLR2 agonists associated with S. pneumoniae.
C4水平降低可能使个体易感染包膜细菌以及引发自身免疫。在本研究中,我们研究了C4在抵御肺炎链球菌诱导的自身免疫中的作用。用19F血清型肺炎球菌进行轻度呼吸道感染可选择性地诱导未感染的C4基因敲除小鼠产生全身性抗双链DNA IgA,但在C3基因敲除小鼠或野生型小鼠中则不会。用强毒株3型肺炎球菌进行全身攻击也会在免疫的C4基因敲除小鼠中诱导抗双链DNA IgA的产生。值得注意的是,单独接种肺炎球菌多糖(PPS)疫苗可诱导C4基因敲除小鼠产生升高的抗双链DNA IgA水平,且在一些小鼠中可维持数月。这些效应在雌性C4基因敲除小鼠中最为明显。重要的是,免疫诱导的抗双链DNA IgA水平升高与肾脏中IgA沉积增加密切相关。肺炎球菌抗原与双链DNA之间的交叉反应在抗双链DNA IgA的诱导中起部分作用,但也揭示了PPS相关的TLR2激动剂起主要作用。在PPS免疫时给予TLR2/4拮抗剂OxPAPC可完全阻断C4基因敲除小鼠中抗双链DNA IgA的产生,而不会抑制PPS特异性抗体的产生。TLR2激动剂Pam3CSK4同样在C4基因敲除小鼠中诱导抗双链DNA IgA的产生,OxPAPC也可阻止这种产生。TLR4激动剂LPS则没有效果。Pam3CSK4而非LPS还能在体外诱导C4基因敲除小鼠脾脏IgA(+) B细胞产生双链DNA特异性IgA,表明TLR2激动剂可通过B细胞内在机制刺激自身抗体的产生。总的来说,我们的结果表明C4在抑制由与肺炎链球菌相关的交叉反应性抗原和TLR2激动剂引发的自身抗体产生中起重要作用。