Granulocytic myeloid derived suppressor cells expansion during active pulmonary tuberculosis is associated with high nitric oxide plasma level

PLoS ONE

Volumn 10, Issue 4, 2015, Pages

  Daker, Sary El ^a,b,c   Sacchi, Alessandra ^a   Tempestilli, Massimo ^a   Carducci, Claudia ^d   Goletti, Delia ^a   Vanini, Valentina ^a   Colizzi, Vittorio ^c   Lauria, Francesco Nicola ^a   Martini, Federico ^a   Martino, Angelo ^a  

^a NATIONAL INSTITUTE FOR INFECTIOUS DISEASES L SPALLANZANI   (Italy)

^b INSTITUT PASTEUR   (France)

^c UNIVERSITY OF ROME TOR VERGATA   (Italy)

^d SAPIENZA UNIVERSITY OF ROME   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

ARGININE; CELL MARKER; NITRIC OXIDE;

ARTICLE; BLOOD ANALYSIS; BLOOD LEVEL; CELL ASSAY; CELL COMPARTMENTALIZATION; CELL EXPANSION; CELL FUNCTION; CELLULAR IMMUNITY; CONTROLLED STUDY; DISEASE ASSOCIATION; DISEASE MARKER; FEMALE; GRANULOCYTIC MYELOID DERIVED SUPPRESSOR CELL; HUMAN; HUMAN CELL; IMMUNE RESPONSE; IMMUNOMODULATION; LUNG TUBERCULOSIS; LYMPHOCYTE PROLIFERATION; MAJOR CLINICAL STUDY; MALE; MOLECULAR DYNAMICS; SUPPRESSOR CELL; T LYMPHOCYTE; BLOOD; BONE MARROW CELL; CELL PROLIFERATION; GRANULOCYTE; PATHOLOGY;

ARGININE; CELL PROLIFERATION; GRANULOCYTES; HUMANS; MYELOID CELLS; NITRIC OXIDE; TUBERCULOSIS, PULMONARY;

EID: 84928251682     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0123772     Document Type: Article

References (21)

1. Gupta A, Kaul A, Tsolaki AG, Kishore U, Bhakta S. Mycobacterium tuberculosis: immune evasion, latency and reactivation. Immunobiology. 2012; 217: 363-374. doi: 10.1016/j.imbio.2011.07.008 PMID: 21813205
2. Zuñiga J, Torres-García D, Santos-Mendoza T, Rodriguez-Reyna TS, Granados J, Yunis EJ. Cellular and humoral mechanisms involved in the control of tuberculosis. Clin Dev Immunol. 2012;193923. doi: 10.1155/2012/193923 PMID: 22666281
3. Sendide K, Deghmane A, Reyrat J, Talal A, Hmama Z. Mycobacterium bovis BCG Urease Attenuates Major Histocompatibility Complex Class II Trafficking to the Macrophage Cell Surface. Infect Immun. 2004; 72: 4200-4209. PMID: 15213164
4. Rich EA, Torres M, Sada E, Finegan CK, Hamilton BD, Toossi Z. Mycobacterium tuberculosis (MTB)-stimulated production of nitric oxide by human alveolar macrophages and relationship of nitric oxide production to growth inhibition of MTB. Tuber Lung Dis. 1997; 78: 247-255. PMID: 10209679
5. Wadee RH, Kuschke TG, Dooms DG. The inhibitory effects of Mycobacterium tuberculosis on MHC class II expression by monocytes activated with riminophenazines and phagocyte stimulants. Clin Exp Immunol. 1995; 100: 434-439. PMID: 7774052
6. Petruccioli E, Romagnoli A, Corazzari M, Coccia EM, Butera O, Delogu G, et al. Specific T cells restore the autophagic flux inhibited by Mycobacterium tuberculosis in human primary macrophages. J Infect Dis. 2012; 205: 1425-1435. doi: 10.1093/infdis/jis226 PMID: 22457295
7. Goletti D, Petruccioli E, Romagnoli A, Piacentini M, Fimia GM. Autophagy in Mycobacterium tuberculosis infection: a passepartout to flush the intruder out? Cytokine Growth Factor Rev. 2013; 24: 335-343. doi: 10.1016/j.cytogfr.2013.01.002 PMID: 23395260
8. Singh SB, Davis AS, Taylor GA, Deretic V. Human IRGM induces autophagy to eliminate intracellular mycobacteria. Science. 2006; 313: 1438-1441. PMID: 16888103
9. Romagnoli A, Etna MP, Giacomini E, Pardini M, Remoli ME, Corazzari M, et al. ESX-1 dependent impairment of autophagic flux by Mycobacterium tuberculosis in human dendritic cells. Autophagy. 2012; 8: 1357-1370. doi: 10.4161/auto.20881 PMID: 22885411
10. Herzmann C, Ernst M, Ehlers S, Stenger S, Maertzdorf J, Sotgiu G, et al. Increased frequencies of pulmonary regulatory T-cells in latent Mycobacterium tuberculosis infection. Eur Respir J. 2012; 40: 1450-1457. doi: 10.1183/09031936.00214611 PMID: 22441737
11. Young MR, Newby M, Wepsic HT. Hematopoiesis and Suppressor Bone Marrow Cells in Mice Bearing Large Metastatic Lewis Lung Carcinoma Tumors. Cancer Res. 1987; 47: 100-105. PMID: 2947676
12. Greten TF, Manns MP, Korangy F. Myeloid derived suppressor cells in human diseases. Int Immunopharmacol. 2011; 11: 802-807. doi: 10.1016/j.intimp.2011.01.003 PMID: 21237299
13. Ochoa AC, Zea AH, Hernandez C, Rodriguez PC. Arginase, prostaglandin and myeloid derived suppressor cells in renal cell carcinoma. Clin Cancer Res. 2007; 13: 761-726.
14. Almand B, Clark JI, Nikitina E, Van Beynen J, English NR, Knight SC, et al. Increse production of immature myeloid cells in cancer patiets: a machanism of immunosuppression in cancer. J Immunol. 2001; 166: 678-689. PMID: 11123353
15. Bronte V, Zanovello P. Regulation of immune responses by L-arginine metabolism. Nat Rev Immunol. 2005; 5: 641-54. PMID: 16056256
16. Yang B, Wang X, Jiang J, Zhai J, Cheng X. Identification of CD-244-expressing myeloid-derived suppressor cells in patients with active tuberculosis. Immunol Lett. 2014; 158: 66-72. doi: 10.1016/j.imlet.2013.12.003 PMID: 24333340
17. Obregon-Henao A, Henao-Tamayo M, Orme IM and Ordway DJ. Gr1(int)CD11b+ myeloid-derived suppressor cells in Mycobacterium tuberculosis infection. PLoS One. 2013; 8: e80669. doi: 10.1371/journal.pone.0080669 PMID: 24224058
18. Du Plessis N, Loebenberg L, Kriel M, Von Groote-Bidlingmaier F, Ribechini E, Loxton AG, et al. Increased frequency of myeloid-derived suppressor cells during active tuberculosis and after recent mycobacterium tuberculosis infection suppresses T-cell function. Am J Respir Crit Care Med. 2013; 188: 724-32. doi: 10.1164/rccm.201302-0249OC PMID: 23885784
19. El Daker S, Sacchi A, Montesano C, Altieri, Galluccio G, Colizzi V, et al. An abnormal phenotype of lung Vγ9Vδ2 T cells impairs their responsiveness in tuberculosis patients. Cell Immunol. 2013; 282: 106-112. doi: 10.1016/j.cellimm.2013.05.001 PMID: 23770719
20. Schuster R. Determination of amino acids in biological, pharmaceutical, plant and food samples by automated precolumn derivatization and high-perfomance liquid chromatography. J Chromatogr. 1998; 43: 271-84.
21. Chiacchio T, Petruccioli E, Vanini V, Butera O, Cuzzi G, Petrone L, et al. Higher frequency of T cell response to M. tuberculosis latency antigen Rv2628 at the site of active tuberculosis disease than in peripheral blood. PLoS One. 2011; 6: e27539. doi: 10.1371/journal.pone.0027539 PMID: 22102905