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Decrease in CD4+CD25+FoxP3+ Treg cells after pulmonary resection in the treatment of cavity multidrug-resistant tuberculosis

Ying E. Wua, Wen Guang Pengb, Ying Mu Caia, Gao Zhe Zhenga, Geng Long Zhengc, Jing Hua Lina, Su Wei Zhanga, Ke LidCorresponding Author Informationemail address

Received 21 September 2009; received in revised form 3 February 2010; accepted 6 April 2010. published online 23 July 2010.
Corrected Proof

Summary 

Objectives

Immune regulatory mechanisms may limit the immunopathologic condition of infection with Mycobacterium tuberculosis and suppress cellular immune responses in the host. We investigated the CD4+CD25+FoxP3+ circulating regulatory T cells (Treg) in patients with cavity multidrug-resistant tuberculosis (MDR-TB) before and after surgery.

Methods

We compared the proportion of Treg cells in 13 patients with cavity MDR-TB pre- and postoperatively and in 10 healthy control subjects by flow cytometry using three specific markers in peripheral blood lymphocytes: cell-surface CD4 and CD25 expression and intracellular FoxP3 expression.

Results

The proportion of CD4+CD25high and CD4+CD25+FoxP3+ Treg was significantly higher in patients with cavity MDR-TB and at 1-month postoperatively than in healthy controls (p<0.001). The proportion of CD4+ and CD4+CD25 cells was significantly lower in patients with cavity MDR-TB than in controls (p<0.001). Pre- and postoperative proportions of CD4+CD25high and CD4+CD25+FoxP3+ Treg cells showed a positive correlation (r=0.878, p<0.001).

Conclusion

Circulating Treg cells are increased in proportion in patients with cavity MDR-TB and decreased after surgery. Infection with M. tuberculosis may induce Treg cell-surface molecular changes with increased numbers of cells.

a Department of Laboratory Medicine, the First Affiliated Hospital of Shantou University Medical College, Shantou, Guangdong, China

b Department of Thoracic Medicine, The Third People's Hospital of Shantou City, Guangdong, China

c Guangdong Key Laboratory of Medical Molecular Imaging, Shantou University Medical College, Shantou, Guangdong, China

d Department of Preventive Medicine, Shantou University Medical College, Xinling Road 22, Shantou, Guangdong, 515031, China

Corresponding Author InformationCorresponding author. Tel.: +86 754 88900445; fax: +86 754 88557562.

PII: S1201-9712(10)02411-2

doi:10.1016/j.ijid.2010.04.005