Mixed inflammatory/regulatory cytokine profile marked by simultaneous raise of interferon-γ and interleukin-10 and low frequency of tumour necrosis factor-α+ monocytes are hallmarks of active human visceral Leishmaniasis due to Leishmania chagasi infection

Author:

Peruhype-Magalhães V123,Martins-Filho O A1,Prata A4,Silva L De A4,Rabello A5,Teixeira-Carvalho A136,Figueiredo R M7,Guimarães-Carvalho S F8,Ferrari T C A9,Van Weyenbergh J10,Correa-Oliveira R3

Affiliation:

1. Laboratório de Doença de Chagas, CPqRR-FIOCRUZ/BH, Brazil

2. Instituto Oswaldo Cruz, FIOCRUZ/RJ, Brazil

3. Laboratório de Imunologia Celular e Molecular, CPqRR-FIOCRUZ/BH, Brazil

4. Faculdade de Medicina do Triângulo Mineiro, Uberaba/MG, Brazil

5. Laboratório de Pesquisas Clínicas, CPqRR-FIOCRUZ/BH, Brazil

6. Escola de Farmácia, Universidade Federal de Ouro Preto/UFOP, Brazil

7. Centro Geral de Pediatria, FHEMIG/BH, Brazil

8. Universidade Estadual de Montes Claros, Montes Claros/MG, Brazil

9. Faculdade de Medicina, UFMG, Belo Horizonte/MG, Brazil

10. Centro de Pesquisas Gonçalo Moniz, FIOCRUZ/BA, Brazil

Abstract

Summary Considering the complexity of the immunological events triggered during active visceral Leishmaniasis (VL), the relevance of the segregation of the immune response during human VL into type 1 and type 2 still remains unclear. For this purpose, in individuals living in risk areas for VL, we have evaluated especially asymptomatic individuals and patients with active VL, the plasmatic levels of cytokines and reactive nitrogen species under ex vivo conditions. In addition, we have also performed an analysis of intracellular cytokine patterns of circulating leucocytes after short-term culture, particularly in the absence of antigenic-specific stimulation, in order to reflect dynamic events of immune response in vivo during Leishmania chagasi infection. Although asymptomatic individuals and non-infected subjects presented a similar immunological profile, an outstanding inflammatory/regulatory profile, based on higher plasmatic levels of cytokines such as interleukin (IL)-8, interferon (IFN)-γ, tumour necrosis factor (TNF)-α, IL-6 and IL-10, was associated with clinical status observed in active VL. In this context, we hypothesize that IL-10, through its ability to inhibit anti-leishmanial macrophage activation, associated with the lower frequency of TNF-α+ monocytes and ordinary levels of nitrite and nitrate are the major mechanisms associated with disease onset.

Publisher

Oxford University Press (OUP)

Subject

Immunology,Immunology and Allergy

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