Selective depression of interferon-gamma and granulysin production with increase of proliferative response by Vgamma9/Vdelta2 T cells in children with tuberculosis

• Published in: The Journal of infectious diseases Vol. 186; no. 12; pp. 1835 - 1839
• Main Authors: Dieli, Francesco, Sireci, Guido, Caccamo, Nadia, Di Sano, Caterina, Titone, Lucina, Romano, Amelia, Di Carlo, Paola, Barera, Annalisa, Accardo-Palumbo, Antonia, Krensky, Alan M, Salerno, Alfredo
• Format: Journal Article
• Language: English
• Published: United States 15.12.2002
• Subjects: Adolescent; Antigens, Differentiation, T-Lymphocyte - biosynthesis; Antitubercular Agents - therapeutic use; Child; Child, Preschool; Female; Humans; Infant; Interferon-gamma - biosynthesis; Male; Mycobacterium tuberculosis; Receptors, Antigen, T-Cell, gamma-delta - analysis; T-Lymphocytes - immunology; Tuberculin Test; Tuberculosis - blood; Tuberculosis - drug therapy; Tuberculosis - immunology
• ISSN: 0022-1899

Vgamma9/Vdelta2 T cells can contribute to protective immune response against Mycobacterium tuberculosis, although the extent to which and mechanisms by which they could actually protect against human tuberculosis remain unclear. We have previously reported that Vgamma9/Vdelta2 T cells from tuberculin purified protein derivative (PPD)-positive children, either healthy or affected by different clinical forms of tuberculosis, strongly proliferate to different phosphoantigens in vitro, whereas Vgamma9/Vdelta2 T cells from PPD-negative healthy subjects proliferate very poorly. We report here that Vgamma9/Vdelta2 T cells from tuberculous children have an increased proliferative activity, but decreased interferon (IFN)-gamma production and granulysin expression. After successful chemotherapy, the Vgamma9/Vdelta2 T cell proliferative response strongly decreased, whereas IFN-gamma and granulysin production consistently increased. Disease-associated changes in Vgamma9/Vdelta2 T cell effector functions in patients with tuberculosis are consistent with the possibility that these T cells may play a protective role in immune response against M. tuberculosis infection.