Perbedaan Antara Jumlah Sel T Subset Gamma-Delta di Darah Tepi pada Penderita Tuberkulosis dan Orang dengan Latent Tuberculosis Infection
Downloads
Abstrak
Latar Belakang. Imunitas memiliki peranan penting untuk melindungi host dari bacilli Mycobacterium tuberculosis (M.tb), bakteri Obligat intraseluler yang menyebabkan Tuberkulosis (TB) dan latent tuberculosis infection (LTBI). Sel T subset gamma-delta (T-γδ) adalah sel-sel potensial tersembunyi yang bermain peran di imunitas innate dan adaptive pada TB. Tetapi, hingga kini perananya di LTBI masih menjadi misteri. Bahan dan Metode. Penelitian dilakukan dengan melibatkan 10 penderita TB serta 10 orang dengan LTBI. Mereka didapatkan dari Rumah Sakit Paru Surabaya melalui suatu persetujuan kelaikan etik dari Universitas Airlangga. Sampel-sampel tersebut akan dihitung jumlah sel T-γδ menggunakan F A C S C a l i b u r. Hasil. Jumlah sel T-γδ meningkat pada TB (10,7%) dan LTBI (15, 4%). Jumlah dari kedua kelompok tersebut melebihi rerata normal di darah tepi (1% - 5%). Kesimpulan. Penigkatan jumlah sel T-γδ pada TB disebabkan melimpahnya kadar IL-12 yang dilepas oleh makrofag selama infeksi. Sementara, peningkatan jumlah sel T-γδ pada LTBI diasumsikan karena banyaknya heat shock protein (HSPs) yang dilepas oleh M.tb di bawah kondisi stres. ...
Kata kunci: tuberkulosis, latent tuberculosis infection, Mycobacterium tuberclosis, sel T subset gamma-d e l t a.
Daftar Pustaka
赤巔清å [Akagawa K]. 2012. çµæ ¸ã®å…ç–« [Imunitas Tuberkulosis]. Kekkaku, 2: 61-70.
Briken V, Porcelli SA, Besra GS, Kremer L. 2004. Mycobacterial Lipoarabinomannan and Related Lipoglycans: from Biogenesis to Modulation of the Immune Response. Mol. Microbiol, 35: 391-403.
Caccamo N, Meraviglia S, Ferlazzo V et al. 2005. Differential Requirement for Antigen of Homeostatic Cytokine for Proliferation and Differentiation of Human Vγ9Vδ2 Naive, Memory, and Effector T Cell Subsets. Eur. J. Immunol, 35: 1764-1772.
Cassetti R, Martino A. 2008. The Plasticity of Gamma-Delta T Cells: Innate Immunity, Antigen Presentation, and New Immunotherapy. Cell. Mol. Immunol, 5: 161-170.
Chan J, Flynn JL. 2004. The Immunological Aspects of Latency in Tuberculosis. Clin. Immunol, 110: 2-12.
Derrick SC, Morris SL. 2007. The ESAT-6 Protein of Mycobacterium tuberculosis Induces Apoptosis of Macrophages by Activating Capsase Expression. Cell. Microbiol, 9: 1547-1555.
Co DO, Hogan LH, Kim SI, Sandor M. 2004. Mycobacterial Granulomas: Keys to a Long-Lasting Host-Pathogen Relationship. Clin. Immunol, 113: 130-136.
Druszczynska M, Kowalewich0Kulbat M, Pol M, Wlodarczyk M, Rudnicka W. 2012. Latent M. tuberculosis Infection – Pathogenesis, Diagnosis, Treatment, and Prevention Strategies. PJM, 61: 3-10.
Dye C, Scheele S, Dolin P, Pathania V, Raviglione MC. 1999. Consensus Statement. Global Burden of Tuberculosis: Estimated Insidence, Prevalence, and Mortality by County. JAMA, 282: 677-686.
Dyrhol-Riise AM, Gran G, Wentzel-Larsen T, Bloomberg B, Haanshuus CG, Morkve O. 2010. Diagnosis and Follow-up of Treatment of Latent Tuberculosis: The Utility of the QuantiFERON TB Gold in-Tube Assay in Outpatients Form a Tuberculosis Low-Endemic Country. BMC. Infect. Dis, 10: 57-65.
Gertner J, Scotet M, Poupot M, Bonneville M, Fournie JJ. 2007. Lymphocytes: Gamma-Delta. In: Roitt's Essential Immunology, 12th Edition. Encyclopedia of Life Science. pp. 1-10. Available in: www.roitt.com/elspdf/lymphocytes_gamma_delta.pdf.
Gideon HP, Flynn JL. 2011. Latent Tuberculosis: What the Host ‘Sees'? Immunol. Res, 50: 202-212.
Gober HJ, Kistowska M, Angman L, Jeno P, Mori L, de Libero G. 2003. Human T Cell Receptor Gammadelta T Cells Recognize Endogenous Mevalonate Metabolites in Tumor Cells. J. Exp. Med, 197: 163-168.
Gogoi D, Chiplunkar SV. 2013. Targeting Gamma-Delta T Cells for Cancer Immunotherapy: Bench to Bedside. IJMR, 138: 755-761.
Grosset J. 2003. Mycobacterium tuberculosis in the Extracellular Compart-ment: an Underestiated Adversary. Antimicrob. Agents. Chemother, 47: 833-836.
Hanekom WA, Mendillo M, Manca C et al. 2003. Mycobacterium tuberculosis Inhibits Maturation of Human Monocyte-Derived Dendritic Cells in Vitro. J. Infect. Dis, 188: 257-266.
Hartmann P, Becker R, Franzen C et al. 2001. Phagocytosis and Killing of Mycobacterium avium Complex by Human Neutrophils. J. Leuko. Bio, 69: 397-404.
Itohara S, Farr AG, Lafaille JJ, Bonneville M, Takagaki Y, Haas W, Tonegawa S. 1990. Homing of Gamma-Delta Thymocyte Subset with Homogenous T-Cell Receptors to Mucosal Epithelial. Nature, 343: 754-757.
Jensen KD, Su X, Shin S et al. 2008. Thymic Selection Determines Gamma-Delta T Cell Effector Fate: Antigen-Naive Cells Make Interleukin-17 and Antigen-Experienced Cells Make Interferon Gamma. Immunity, 29: 90-100.
Junqueira-Kipnis AP, Kipnis A, Jamieson A, Juarerro MG, Diefenbach A, Raulet DH, Turner J, Orme IM. 2003. NK Cells Respond to Pulmonary Infection with Mycobacterium tuberculosis, but Play a Minimal Role in Protection. J. Immunol, 171: 6039-6045.
Kaufmann SHE. 2012. Mycobacterium tuberculosis: Success Through Dormancy. FEMS. Microbiol. Rev, 36: 514-532.
Kawai T, Akira S. 2010. The Role of Pattern-Recognition Receptors in Innate Immunity: Update on Toll-like Receptors. Nat. Rev. Immun, 11: 373-384.
Kinhikar AG, Verma I, Chandra D et al. 2010. Potential Role for ESAT-6 in Dissemination of M. tuberculosis via Human Lung Epithelial Cells. Mol. Microbiol, 75: 92-106.
Means TK, Wang S, Lien E, Yoshimura A, Golenbock DT, Fenton MJ. 1999. Human Toll-like Receptors Mediate Cellular Activation by Mycobacterium tuberculosis. J. Immunol, 163: 3920-3927.
Murugaiyan G and Saha B. 2008. Protumor vs Antitumor Function of IL-17. J. Immunol, 183: 4169-4175.
O'Brien RL, Happ MP, Dallas A, Palmer E, Kubo R, Born WK. 1989. Stimulation of a Major Subset of Lymphocytes Expressing T Cell Receptor Gamma-Delta by an Antigen Derived from Mycobacterium tuberculosis, Cell, 57: 667-674.
Ogata K, Linzer BA, Zuberi RI, Ganz T, Lehrer RI, Catanzaro A. 1992. Activity of Defensins from Human Neutrophilic Granulocytes Againts Mycobacterium avium – Mycobacterium intracellulare. Infect Immun, 60: 4720-4725.
Peyron P, Vaubourgeix J, Poquet Y et al. 2008. Foamy Macrophages from Tuber-culosis Patients Granulomas Constitute a Nutrient-Rich Reservoir for M. tuberculosis Persistence. PLoS. Pathog, 4: 100204.
Serbina NV, Lazarevic V, Flynn JL. 2001. CD4+ T Cells are Required for the Development of Cytotoxic CD8+ T Cells during Mycobacterium tuberculosis Infection. J. Immunol, 167: 6991-7000.
Shibata K. 2012. Close Link Between Development and Function of Gamma-Delta T Cells. Microbiol. Immunol, 56: 217-227.
Turcinovich G, Hayday AC. 2011. Skint-1 Identifies a Common Molecular Mechanism for the Development of Interferon-Gamma-Secreting versus Interlekin-17-Secreting Gamma-Delta T Cells. Immunity, 35: 59-68.
Umemura M, Yahagi A, Hamada S, Watanabe H, Kawakami K, Suda T, Sudo K, Nakae S, Iwakra Y, Matsuzaki G. 2007. IL-17-Mediated Regulation of Innate and Acquired Immune Response Againts Pulmonary Mycobacterium bovis Bacillus Calmette-Guerin Infection. J. Immunol, 178: 3786, 3796.
WHO. 2015. Global Tuberculosis Report. Genewa: World Health Organization. pp. 1-134. Available in: http://www.who.int/tb/publications/global_report/gtbr15_main_text.pdf.
Authors who publish with this journal agree to the following terms:
- The copyright of this journal belongs to the Editorial Board and Journal Manager with the author's knowledge, while the moral right of the publication belong to the author.
- The formal legal aspect of journal publication accessibility refers to the Creative Commons Attribution-Share Alike (CC BY-SA).
- Every publication (print/electronic) is open access for educational, research, and library purposes. In addition to the objectives mentioned above, the editorial board is not responsible for copyright infringement