Thye Thorsten, Scarisbrick Genevieve, Browne Edmund N L, Chinbuah Margaret Amanua, Gyapong John, Osei Ivy, Owusu-Dabo Ellis, Niemann Stefan, Rüsch-Gerdes Sabine, Meyer Christian G, Horstmann Rolf D
Department of Molecular Medicine, Bernhard Nocht Institute for Tropical Medicine, Hamburg, Germany.
PLoS One. 2009 Jul 17;4(7):e6307. doi: 10.1371/journal.pone.0006307.
The gene of Cytotoxic T Lymphocyte-associated Antigen 4 (CTLA4), a negative regulator of T lymphocytes, contains a single-nucleotide polymorphism (SNP) at position +6230A->G (ct60A->G), which has been found associated with several autoimmune diseases and appears to reduce T-cell inhibitory activity. In Ghana, West Africa, we compared the frequencies of CTLA4 +6230 A/G and 6 haplotype-tagging SNPs in 2010 smear-positive, HIV-negative patients with pulmonary tuberculosis (TB) and 2346 controls matched for age, gender and ethnicity. We found no difference in allele frequencies between cases and controls. However, +6230A and a distinct CTLA4 haplotype and a diplotype comprising the +6230A allele were significantly less frequent among cases with large opacities in chest radiographs compared to those with small ones (P(corrected [cor]) = 0.002, P(cor) = 0.00045, P = 0.0005, respectively). This finding suggests that an increased T-cell activity associated with the CTLA4 +6230G allele contributes to pathology rather than to protection in pulmonary TB.
细胞毒性T淋巴细胞相关抗原4(CTLA4)是T淋巴细胞的负调节因子,其基因在+6230A→G(ct60A→G)位置存在单核苷酸多态性(SNP),已发现该多态性与多种自身免疫性疾病相关,且似乎会降低T细胞抑制活性。在西非的加纳,我们比较了2010例涂片阳性、HIV阴性的肺结核(TB)患者与2346例年龄、性别和种族匹配的对照中CTLA4 +6230 A/G及6个单倍型标签SNP的频率。我们发现病例组和对照组的等位基因频率没有差异。然而,与胸片上有小阴影的病例相比,胸片上有大阴影的病例中+6230A以及一个独特的CTLA4单倍型和包含+6230A等位基因的双倍型的频率显著更低(校正后P[cor]=0.002,P[cor]=0.00045,P = 0.0005)。这一发现表明,与CTLA4 +6230G等位基因相关的T细胞活性增加在肺结核中促进了病理过程而非起到保护作用。