Keogan M T, Callaghan M, Yanni G, Mulherin D, Feighery C, Brown D L, Fitzgerald M X, Bresnihan B
Department of Respiratory Medicine (Adult Cystic Fibrosis Unit, University College, Dublin, Ireland.
Clin Exp Immunol. 1993 Mar;91(3):462-6. doi: 10.1111/j.1365-2249.1993.tb05925.x.
Rheumatoid factor (RF) production has been demonstrated during infections, including infectious exacerbations of cystic fibrosis (CF). The aim of this study was to evaluate the relationship of RF production to infection, and examine the mechanisms involved. Serial peripheral blood mononuclear cell (PBMC) cultures with measurement of spontaneous production of IgM RF, IgA RF, total IgM and IgA, and measurement of serum levels of immune complexes were carried out during exacerbations of CF. The percentage of B cells expressing CD5 was examined in a second cohort of acutely infected CF patients, and related to IgM RF production. IgM RF production was significantly elevated during acute infection compared with convalescence (P < 0.05), stable CF subjects (P < 0.005) and normal controls (P < 0.05). IgM RF production did not correlate with total IgM production in the majority of patients, but was closely related to circulating immune complex levels in 8/10 subjects. IgA RF production did not increase significantly during infection, and did not correlate with total IgA or IgM RF production, or with circulating immune complex levels. CD5+ B cells were not increased in the CF group, and the percentage of CD5+ B cells did not correlate with IgM RF synthesis. These observations suggest that RF production during infection is specifically induced, possibly by immune complex autoimmunization, and is not simply the result of polyclonal B cell activation. Different patterns of IgM RF and IgA RF synthesis suggest different mechanisms of induction.
类风湿因子(RF)的产生已在感染过程中得到证实,包括囊性纤维化(CF)的感染性加重期。本研究的目的是评估RF产生与感染的关系,并探讨其中涉及的机制。在CF加重期进行系列外周血单个核细胞(PBMC)培养,检测自发产生的IgM RF、IgA RF、总IgM和IgA,并检测血清免疫复合物水平。在另一组急性感染的CF患者中检测表达CD5的B细胞百分比,并将其与IgM RF产生相关联。与恢复期(P < 0.05)、稳定期CF患者(P < 0.005)和正常对照(P < 0.05)相比,急性感染期间IgM RF产生显著升高。在大多数患者中,IgM RF产生与总IgM产生无关,但在8/10的受试者中与循环免疫复合物水平密切相关。感染期间IgA RF产生未显著增加,且与总IgA或IgM RF产生以及循环免疫复合物水平均无相关性。CF组中CD5 + B细胞未增加,CD5 + B细胞百分比与IgM RF合成无关。这些观察结果表明,感染期间RF的产生是特异性诱导的,可能是由免疫复合物自身免疫引起的,而不仅仅是多克隆B细胞激活的结果。IgM RF和IgA RF合成的不同模式提示了不同的诱导机制。