, 2009). However, very little is known about the interaction of PMN with vaccine strains of mycobacteria. As neutrophils are the first cells to get exposed to any antigen and generate early immune response, their interaction with vaccine strains will help us to understand the exact nature of protective immune response. Hence, we studied in vitro modulation of neutrophil functions like phenotypic changes, apoptosis rate, and inflammatory

cytokines after infection with vaccine strains (BCG and Mw) and compared with standard laboratory strain H37Rv. To understand the paracrine c-Met inhibitor role of neutrophils and their influence on mononuclear cell recruitment, we also studied the expression profile of the activation markers and chemokine receptors on T cells and monocytes. The study protocol was approved by the institutional ethical committee and followed the institute check details ethical guidelines. Written informed consents were obtained from blood donors, and 10 mL of heparinized blood was collected through venipuncture. The study group consisted of normal healthy volunteers (N = 11) (mean age 24 years, range 22–28 years) who received BCG vaccination in childhood, but their tuberculin skin test status was unknown. They showed no clinical signs and symptoms of tuberculosis or any other immunosuppressive

diseases at the time of blood sampling. Two vaccine strains, namely BCG and Mw, available in India were used. The standard laboratory strain live H37Rv was used for comparison. Live, attenuated BCG vaccine was purchased from Serum institute of India, Chennai. Heat-killed Mw vaccine was purchased from Cadila

pharmaceuticals Limited, Ahmedabad. Colonies of H37Rv from Lowenstein-Jensen-slopes were inoculated in Sauton’s medium and grown as standing cultures at 37 °C. Log-phase cultures were centrifuged and washed with phosphate-buffered saline (PBS) (Biowhittaker, Belgium), and bacterial clumps were dispersed by passing them through 26-gauge needle. The bacterial suspension was centrifuged Ixazomib to remove the remaining clumps, and the supernatant containing the single-cell suspension was adjusted to 5 × 107 cells mL−1 in sterile, endotoxin-free PBS and stored in aliquots at −70 °C until use. The viability of bacilli was enumerated by CFU values. Human neutrophils were isolated by standard protocol (Böyum, 1968). Briefly, heparinized venous blood was layered over Ficoll-Hypaque (Amersham Biosciences) for gradient centrifugation followed by sedimentation in 3% dextran (Sigma Chemicals). The PMN rich supernatant was collected, and the residual RBCs were lysed by hypotonic lysis. The cells were washed and resuspended in RPMI 1640 (Gibco BRL, CA) supplemented with 1% fetal bovine serum (FBS) (Gibco BRL). The viability of the cells was assessed to be > 95% by the trypan blue exclusion test, and the purity was always found to be > 90%. The cell density was adjusted to 0.5 × 106 cells mL−1.