Mediators of Inflammation

Mediators of Inflammation / 2006 / Article

Review Article | Open Access

Volume 2006 |Article ID 089070 | https://doi.org/10.1155/MI/2006/89070

Figen Deveci, H. Handan Akbulut, Ilhami Celik, M. Hamdi Muz, Fulya İlhan, "Lymphocyte Subpopulations in Pulmonary Tuberculosis Patients", Mediators of Inflammation, vol. 2006, Article ID 089070, 6 pages, 2006. https://doi.org/10.1155/MI/2006/89070

Lymphocyte Subpopulations in Pulmonary Tuberculosis Patients

Received23 Dec 2005
Revised09 Jan 2006
Accepted20 Jan 2006
Published19 Mar 2006

Abstract

Protection against Mycobacterium tuberculosis is based on cell-mediated immunity, most importantly involving CD4+ and CD8+ T-cell subsets. The aim of this study was to evaluate CD4+ and CD8+ T-cell profiles and CD19+ and CD3-CD(16+56)+ populations in patients with pulmonary tuberculosis. CD4+ and CD8+ T cells, B-lymphocytes, and natural killer (NK) cells were evaluated in 75 active (APTB) and 25 inactive (IPTB) pulmonary tuberculosis cases and 20 healthy subjects (HCs). The results were compared at different stages of antituberculosis treatment in the APTB patients and also according to X-ray findings in the newly diagnosed APTB patients. The percentages of CD4+ T cells were significantly lower (P<.01) and those of CD3-CD(16+56)+ cells were significantly higher (P<.01) in APTB patients than in HCs. CD8+ T cells were significantly decreased (P<.05), and CD3-CD(16+56)+ cells were significantly increased (P<.01), in IPTB patients compared to HCs. The percentages of CD4+, CD8+, CD3-CD19+, and CD3-CD(16+56)+ cells showed no differences at different times of the antituberculosis regimen, and different stages of newly diagnosed APTB patients. APTB patients have a reduced percentage of circulating CD4+ T cells and an increased percentage of NK cells compared with healthy individuals. These cells could play important roles in the immune response to M tuberculosis infection.

References

  1. W H Boom, D H Canaday, S A Fulton, A J Gehring, R E Rojas, and M Torres, “Human immunity to M. tuberculosis: T cell subsets and antigen processing,” Tuberculosis (Edinburgh), vol. 83, no. 1–3, pp. 98–106, 2003. View at: Google Scholar
  2. J Talreja, A Bhatnagar, S K Jindal, and N K Ganguly, “Influence of Mycobacterium tuberculosis on differential activation of helper T-cells,” Clinical and Experimental Immunology, vol. 131, no. 2, pp. 292–298, 2003. View at: Google Scholar
  3. J A Pilheu, M C De Salvo, J Gonzalez, D Rey, M C Elias, and M C Ruppi, “CD4+ T-lymphocytopenia in severe pulmonary tuberculosis without evidence of human immunodeficiency virus infection,” The International Journal of Tuberculosis and Lung Disease, vol. 1, no. 5, pp. 422–426, 1997. View at: Google Scholar
  4. D Dlugovitzky, A Torres-Morales, L Rateni et al., “Circulating profile of Th1 and Th2 cytokines in tuberculosis patients with different degrees of pulmonary involvement,” FEMS Immunology and Medical Microbiology, vol. 18, no. 3, pp. 203–207, 1997. View at: Google Scholar
  5. American Thoracic Society, “Diagnostic standard and classification of tuberculosis,” The American Review of Respiratory Disease, vol. 142, pp. 725–735, 1990. View at: Google Scholar
  6. J Montes Santiago, F Gambon Deza, M Pacheco Carracedo, and T Cerda Mota, “Cellular immune response in tuberculosis: analysis of T-lymphocytes and their subsets, B-lymphocytes and natural cytotoxic cells in different tuberculosis states and body fluids,” Revista Clinica Espanola, vol. 196, no. 4, pp. 223–227, 1996. View at: Google Scholar
  7. B E Jones, M M Oo, E K Taikwel et al., “CD4 cell counts in human immunodeficiency virus-negative patients with tuberculosis,” Clinical Infectious Diseases, vol. 24, no. 5, pp. 988–991, 1997. View at: Google Scholar
  8. I M Orme, P Andersen, and W H Boom, “T cell response to Mycobacterium tuberculosis,” The Journal of Infectious Diseases, vol. 167, no. 6, pp. 1481–1497, 1993. View at: Google Scholar
  9. C T Yu, C H Wang, T J Huang, H C Lin, and H P Kuo, “Relation of bronchoalveolar lavage T lymphocyte subpopulations to rate of regression of active pulmonary tuberculosis,” Thorax, vol. 50, no. 8, pp. 869–874, 1995. View at: Google Scholar
  10. A C Carvalho, A Matteelli, P Airo et al., “gamma/delta T lymphocytes in the peripheral blood of patients with tuberculosis with and without HIV co-infection,” Thorax, vol. 57, no. 4, pp. 357–360, 2002. View at: Google Scholar
  11. J K Onwubalili, A J Edwards, and L Palmer, “T4 lymphopenia in human tuberculosis,” Tubercle, vol. 68, no. 3, pp. 195–200, 1987. View at: Google Scholar
  12. G M Ainslie, J A Solomon, and E D Bateman, “Lymphocyte and lymphocyte subset numbers in blood and in bronchoalveolar lavage and pleural fluid in various forms of human pulmonary tuberculosis at presentation and during recovery,” Thorax, vol. 47, no. 7, pp. 513–518, 1992. View at: Google Scholar
  13. M D Ashtekar, A M Samuel, G V Kadival, V Sakhalkar, S Rajadhyaksha, and S S Virdi, “T lymphocytes in pulmonary tuberculosis,” The Indian Journal of Medical Research, vol. 97, pp. 14–17, 1993. View at: Google Scholar
  14. M Singhal, J N Banavalikar, S Sharma, and K Saha, “Peripheral blood T lymphocyte subpopulations in patients with tuberculosis and the effect of chemotherapy,” Tubercle, vol. 70, no. 3, pp. 171–178, 1989. View at: Google Scholar
  15. N Shijubo, F Nakanishi, M Hirasawa et al., “Phenotypic analysis in peripheral blood lymphocytes of patients with pulmonary tuberculosis,” Kekkaku, vol. 67, no. 9, pp. 581–585, 1992 (Japanese). View at: Google Scholar
  16. P Yildiz, F Kadakal, Y Tutuncu et al., “Natural killer cell activity in multidrug-resistant pulmonary tuberculosis,” Respiration, vol. 68, no. 6, pp. 590–594, 2001. View at: Google Scholar
  17. G S Turett and E E Telzak, “Normalization of CD4+ T-lymphocyte depletion in patients without HIV infection treated for tuberculosis,” Chest, vol. 105, no. 5, pp. 1335–1337, 1994. View at: Google Scholar
  18. S S Uppal, S C Tewari, S Verma, and P S Dhot, “Comparison of CD4 and CD8 lymphocyte counts in HIV-negative pulmonary TB patients with those in normal blood donors and the effect of antitubercular treatment: hospital-based flow cytometric study,” Cytometry. Part B, Clinical Cytometry, vol. 61, no. 1, pp. 20–26, 2004. View at: Google Scholar
  19. H M Vordermeier, N Venkataprasad, D P Harris, and J Ivanyi, “Increase of tuberculous infection in the organs of B cell-deficient mice,” Clinical and Experimental Immunology, vol. 106, no. 2, pp. 312–316, 1996. View at: Google Scholar
  20. C M Johnson, A M Cooper, A A Frank, C B Bonorino, L J Wysoki, and I M Orme, “Mycobacterium tuberculosis aerogenic rechallenge infections in B cell-deficient mice,” Tubercle and Lung Disease, vol. 78, no. 5-6, pp. 257–261, 1997. View at: Google Scholar
  21. M Corominas, V Cardona, L Gonzalez et al., “B-lymphocytes and co-stimulatory molecules in Mycobacterium tuberculosis infection,” The International Journal of Tuberculosis and Lung Disease, vol. 8, no. 1, pp. 98–105, 2004. View at: Google Scholar
  22. L E Bermudez and L S Young, “Natural killer cell-dependent mycobacteriostatic and mycobactericidal activity in human macrophages,” Journal of Immunology, vol. 146, no. 1, pp. 265–270, 1991. View at: Google Scholar
  23. K V Harshan and P R Gangadharam, “In vivo depletion of natural killer cell activity leads to enhanced multiplication of Mycobacterium avium complex in mice,” Infection and Immunity, vol. 59, no. 8, pp. 2818–2821, 1991. View at: Google Scholar
  24. A P Junqueira-Kipnis, A Kipnis, A Jamieson et al., “NK cells respond to pulmonary infection with Mycobacterium tuberculosis, but play a minimal role in protection,” Journal of Immunology, vol. 171, no. 11, pp. 6039–6045, 2003. View at: Google Scholar
  25. T Yoneda and J J Ellner, “CD4+ T cell and natural killer cell-dependent killing of Mycobacterium tuberculosis by human monocytes,” American Journal of Respiratory and Critical Care Medicine, vol. 158, no. 2, pp. 395–403, 1998. View at: Google Scholar
  26. T Yoneda, M Kasai, J Ishibashi, K Nishikawa, T Tokunaga, and R Mikami, “NK cell activity in pulmonary tuberculosis,” British Journal of Diseases of the Chest, vol. 77, no. 2, pp. 185–188, 1983. View at: Google Scholar
  27. J Qin, “NK cell activity and counts of T-lymphocyte subsets in pulmonary tuberculosis,” Zhonghua Jie He He Hu Xi Za Zhi, vol. 13, no. 4, pp. 209–211, 1990 (Chinese). View at: Google Scholar
  28. S Saenghirunvattana, “CD4 + T counts with a course of antituberculous therapy in healthy and HIV-infected patients,” Journal of the Medical Association of Thailand, vol. 79, no. 4, pp. 246–248, 1996. View at: Google Scholar
  29. R Nirmala, P R Narayanan, R Mathew, M Maran, and C N Deivanayagam, “Reduced NK activity in pulmonary tuberculosis patients with/without HIV infection: identifying the defective stage and studying the effect of interleukins on NK activity,” Tuberculosis (Edinburgh), vol. 81, no. 5-6, pp. 343–352, 2001. View at: Google Scholar
  30. F Morikawa, A Nakano, H Nakano, F Oseko, and S Morikawa, “Enhanced natural killer cell activity in patients with pulmonary tuberculosis,” Japanese Journal of Medicine, vol. 28, no. 3, pp. 316–322, 1989. View at: Google Scholar
  31. R A Taha, T C Kotsimbos, Y L Song, D Menzies, and Q Hamid, “IFN-gamma and IL-12 are increased in active compared with inactive tuberculosis,” American Journal of Respiratory and Critical Care Medicine, vol. 155, no. 3, pp. 1135–1139, 1997. View at: Google Scholar
  32. I V Lyadova, E B Eruslanov, S V Khaidukov et al., “Comparative analysis of T lymphocytes recovered from the lungs of mice genetically susceptible, resistant, and hyperresistant to Mycobacterium tuberculosis-triggered disease,” Journal of Immunology, vol. 165, no. 10, pp. 5921–5931, 2000. View at: Google Scholar

Copyright © 2006 Figen Deveci et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.


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