PLoS ONE (Jan 2009)

CTLA4 autoimmunity-associated genotype contributes to severe pulmonary tuberculosis in an African population.

  • Thorsten Thye,
  • Genevieve Scarisbrick,
  • Edmund N L Browne,
  • Margaret Amanua Chinbuah,
  • John Gyapong,
  • Ivy Osei,
  • Ellis Owusu-Dabo,
  • Stefan Niemann,
  • Sabine Rüsch-Gerdes,
  • Christian G Meyer,
  • Rolf D Horstmann

DOI
https://doi.org/10.1371/journal.pone.0006307
Journal volume & issue
Vol. 4, no. 7
p. e6307

Abstract

Read online

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.