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B族链球菌定植和侵袭性疾病患者中的αC蛋白特异性免疫

Alpha C protein-specific immunity in humans with group B streptococcal colonization and invasive disease.

作者信息

Pannaraj Pia S, Kelly Joanna K, Rench Marcia A, Madoff Lawrence C, Edwards Morven S, Baker Carol J

机构信息

Section of Infectious Diseases, Department of Pediatrics, Baylor College of Medicine and Texas Children's Hospital, Houston, TX 77030, USA.

出版信息

Vaccine. 2008 Jan 24;26(4):502-8. doi: 10.1016/j.vaccine.2007.11.034. Epub 2007 Dec 3.

Abstract

Alpha C protein, found in 76% of non-type III strains of group B Streptococcus (GBS), elicits antibodies protective against alpha C-expressing strains in experimental animals, making it an appealing carrier for a GBS conjugate vaccine. We determined whether natural exposure to alpha C elicits antibodies in women. Geometric mean concentrations of alpha C-specific IgM and IgG were similar by ELISA in sera from 58 alpha C GBS strain colonized and 174 age-matched non-colonized women (IgG 245 and 313 ng/ml; IgM 257 and 229 ng/ml, respectively), but acute sera from 13 women with invasive alpha C-expressing GBS infection had significantly higher concentrations (IgM 383 and IgG 476 ng/ml [p=0.036 and 0.038, respectively]). Convalescent sera from 5 of these women 16-49 days later had high alpha C-specific IgM and IgG concentrations (1355 and 4173 ng/ml, respectively). In vitro killing of alpha C-expressing GBS correlated with total alpha C-specific antibody concentration. Invasive disease but not colonization elicits alpha C-specific IgM and IgG in adults.

摘要

αC蛋白存在于76%的B族链球菌(GBS)非III型菌株中,在实验动物体内能引发针对表达αC的菌株的保护性抗体,这使其成为GBS结合疫苗的一个有吸引力的载体。我们确定了女性自然接触αC是否会引发抗体。通过酶联免疫吸附测定(ELISA),58名定植有αC GBS菌株的女性和174名年龄匹配的未定植女性血清中,αC特异性IgM和IgG的几何平均浓度相似(IgG分别为245和313 ng/ml;IgM分别为257和229 ng/ml),但13名患有侵袭性表达αC的GBS感染的女性的急性期血清浓度显著更高(IgM为383 ng/ml,IgG为476 ng/ml [p分别为0.036和0.038])。其中5名女性在16 - 49天后的恢复期血清中,αC特异性IgM和IgG浓度很高(分别为1355和4173 ng/ml)。体外对表达αC的GBS的杀伤作用与αC特异性总抗体浓度相关。侵袭性疾病而非定植会在成年人中引发αC特异性IgM和IgG。

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