Recruitment of Th1 effector cells in human tuberculosis: Hierarchy of chemokine receptor(s) and their ligands

• Enrichment of CXCR3+CCR5+CD11ahigh T cells in PE and BAL of TB-PE & MTB.
• Highest number of CXCR3+CCR5+ cells among activated lymphocytes in TB-PE.
• CXCR3+CCR5+ cells dominantly produced IFN-γ in response to M. tuberculosis antigens.
• All CCR5+ cells were positive for CXCR3 in PF of TB-PE.
• RANTES and IP-10 are hierarchic in the selective recruitment of CXCR3+CCR5+ cells.

Selective recruitment of IFN-γ biased Th1 effector cells at the pathologic site(s) determines the local immunity of tuberculosis (TB). We observed the enrichment of CXCR3, CCR5 and CD11ahigh T cells in the peripheral blood, pleural fluid and bronchoalveolar lavage of TB pleural effusion (TB-PE) and miliary tuberculosis (MTB) patients respectively. CXCR3+CCR5+ T cells were significantly high at the local disease site(s) in both the forms of TB and their frequency was highest among activated lymphocytes in TB-PE. Interestingly, all CCR5+ cells were invariably positive for CXCR3 but all CXCR3+ cells did not co-express CCR5 in pleural fluid whereas the situation was reverse in bronchoalveolar lavage. These CXCR3+CCR5+ cells dominantly produced IFN-γ in response to Mycobacterium tuberculosis antigen. In vitro chemotaxis assay indicates dominant role of RANTES and IP-10 in the selective recruitment of CXCR3+CCR5+cells at the tubercular pathologic sites.