Apoptotic Mediators in Patients With Severe and Non-Severe Dengue From Brazil

被引:16
作者
Limonta, Daniel [1 ,2 ]
Torrentes-Carvalho, Amanda [1 ]
Marinho, Cintia Ferreira [1 ]
de Azeredo, Elzinandes Leal [1 ]
de Souza, Luiz Jose [3 ]
Motta-Castro, Ana Rita C. [4 ]
da Cunha, Rivaldo Venancio [4 ]
Kubelka, Claire Fernandes [1 ]
Ribeiro Nogueira, Rita Maria [2 ]
de-Oliveira-Pinto, Luzia Maria [1 ]
机构
[1] Fiocruz MS, Inst Oswaldo Cruz, Lab Imunol Viral, BR-21045900 Rio De Janeiro, Brazil
[2] Fiocruz MS, Inst Oswaldo Cruz, Lab Flavivirus, BR-21045900 Rio De Janeiro, Brazil
[3] Ctr Reg Referencia Dengue, Rio De Janeiro, Brazil
[4] Univ Fed Mato Grosso do Sul, Setor Hemonucleo, Cuiaba, MS, Brazil
关键词
apoptosis; pathogenesis; lymphocytes; monocytes; NECROSIS-FACTOR-ALPHA; VIRUS-INDUCED APOPTOSIS; HEMORRHAGIC-FEVER; ENDOTHELIAL-CELLS; DENDRITIC CELLS; LYMPHOCYTE APOPTOSIS; SURVIVIN EXPRESSION; INFECTED PATIENTS; DISEASE SEVERITY; SERUM-LEVELS;
D O I
10.1002/jmv.23832
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Despite being the most significant arboviral disease worldwide, dengue has no antiviral treatment or reliable severity predictors. It has been shown that apoptotic cells from blood and tissues may be involved in the complex pathogenesis of dengue. However, very little is known about the interplay between proapoptotic and antiapoptotic mediators in this disease. Therefore, plasma levels of the three proapoptotic mediators Fas ligand (FasL), tumor necrosis factor-alpha (TNF-alpha), and TNF-related apoptosis-inducing ligand (TRAIL) were measured in dengue patients. Patients were classified according to the World Health Organization classification of dengue revised in 2009. Additionally, inhibitors of apoptosis protein (IAPs) were determined in plasma (Survivin) and peripheral blood mononuclear cells (PBMCs) lysates (cIAP-1, cIAP-2, XIAP). Levels of apoptotic proteins in plasma were correlated with counts of blood cells. FasL and TRAIL levels were elevated in dengue patients without warning signs when compared to patients with severe dengue and controls. Dengue patients with warning signs showed decreased levels of Survivin compared to patients with severe dengue and controls. TRAIL was inversely correlated with counts of lymphocyte subsets. In contrast, Survivin was positively correlated with leukocyte counts. There was a trend of elevated IAPs levels in PBMCs of patients with severe dengue. The results suggest a likely antiviral effect of TRAIL in dengue. It appears that TRAIL might be involved with apoptosis induction of lymphocytes, whereas IAPs might participate in protecting leukocytes from apoptosis. Further research is needed to explore the interactions between pro and antiapoptotic molecules and their implications in dengue pathogenesis. (C) 2013 Wiley Periodicals, Inc.
引用
收藏
页码:1437 / 1447
页数:11
相关论文
共 68 条
[1]   Multicentre prospective study on dengue classification in four South-east Asian and three Latin American countries [J].
Alexander, Neal ;
Balmaseda, Angel ;
Coelho, Ivo C. B. ;
Dimaano, Efren ;
Hien, Tran T. ;
Hung, Nguyen T. ;
Jaenisch, Thomas ;
Kroeger, Axel ;
Lum, Lucy C. S. ;
Martinez, Eric ;
Siqueira, Joao B. ;
Thuy, Tran T. ;
Villalobos, Iris ;
Villegas, Elci ;
Wills, Bridget .
TROPICAL MEDICINE & INTERNATIONAL HEALTH, 2011, 16 (08) :936-948
[2]   Survivin and IAP proteins in cell-death mechanisms [J].
Altieri, Dario C. .
BIOCHEMICAL JOURNAL, 2010, 430 :199-205
[3]  
[Anonymous], 2019, Dengue Guidelines for Diagnosis, Treatment, Prevention and Control
[4]   Differential proinflammatory and angiogenesis-specific cytokine production in human pulmonary endothelial cells, HPMEC-ST1.6R infected with dengue-2 and dengue-3 virus [J].
Azizan, Azliyati ;
Sweat, James ;
Espino, Carlos ;
Gemmer, Jennifer ;
Stark, Lillian ;
Kazanis, Deno .
JOURNAL OF VIROLOGICAL METHODS, 2006, 138 (1-2) :211-217
[5]   Different Innate Signatures Induced in Human Monocyte-derived Dendritic Cells by Wild-Type Dengue 3 Virus, Attenuated but Reactogenic Dengue 3 Vaccine Virus, or Attenuated Nonreactogenic Dengue 1-4 Vaccine Virus Strains [J].
Balas, Claire ;
Kennel, Audrey ;
Deauvieau, Florence ;
Sodoyer, Regis ;
Arnaud-Barbe, Nadege ;
Lang, Jean ;
Guy, Bruno .
JOURNAL OF INFECTIOUS DISEASES, 2011, 203 (01) :103-108
[6]   Serotype-specific differences in clinical manifestations of dengue [J].
Balmaseda, A ;
Hammond, SN ;
Pérez, L ;
Tellez, Y ;
Saborío, SI ;
Mercado, JC ;
Cuadra, R ;
Rocha, J ;
Pérez, MA ;
Silva, S ;
Rocha, C ;
Harris, E .
AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE, 2006, 74 (03) :449-456
[7]   Usefulness and applicability of the revised dengue case classification by disease: multi-centre study in 18 countries [J].
Barniol, Judit ;
Gaczkowski, Roger ;
Vega Barbato, Eliana ;
da Cunha, Rivaldo V. ;
Salgado, Doris ;
Martinez, Eric ;
Soria Segarra, Carmita ;
Pleites Sandoval, Ernesto B. ;
Mishra, Ajay ;
Laksono, Ida Safitri ;
Lum, Lucy C. S. ;
Martinez, Jose G. ;
Nunez, Andrea ;
Balsameda, Angel ;
Allende, Ivan ;
Ramirez, Gladys ;
Dimaano, Efren ;
Thomacheck, Kay ;
Akbar, Naeema A. ;
Ooi, Eng E. ;
Villegas, Elci ;
Hien, Tran T. ;
Farrar, Jeremy ;
Horstick, Olaf ;
Kroeger, Axel ;
Jaenisch, Thomas .
BMC INFECTIOUS DISEASES, 2011, 11
[8]   Gene Expression Profiling of Dengue Infected Human Primary Cells Identifies Secreted Mediators In Vivo [J].
Becerra, Aniuska ;
Warke, Rajas V. ;
Martin, Katherine ;
Xhaja, Kris ;
de Bosch, Norma ;
Rothman, Alan L. ;
Bosch, Irene .
JOURNAL OF MEDICAL VIROLOGY, 2009, 81 (08) :1403-1411
[9]   The global distribution and burden of dengue [J].
Bhatt, Samir ;
Gething, Peter W. ;
Brady, Oliver J. ;
Messina, Jane P. ;
Farlow, Andrew W. ;
Moyes, Catherine L. ;
Drake, John M. ;
Brownstein, John S. ;
Hoen, Anne G. ;
Sankoh, Osman ;
Myers, Monica F. ;
George, Dylan B. ;
Jaenisch, Thomas ;
Wint, G. R. William ;
Simmons, Cameron P. ;
Scott, Thomas W. ;
Farrar, Jeremy J. ;
Hay, Simon I. .
NATURE, 2013, 496 (7446) :504-507
[10]   Pathological survivin expression links viral infections with pathogenesis of erosive rheumatoid arthritis [J].
Bokarewa, M. ;
Tarkowski, A. ;
Magnusson, M. .
SCANDINAVIAN JOURNAL OF IMMUNOLOGY, 2007, 66 (2-3) :192-198