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Published on: July 29, 2012
CD86 Expression by Monocytes Influences an Immunomodulatory Profile in Asymptomatic Patients with Chronic Chagas
Bruna F Pinto1, Nayara I Medeiros1,2, Andrea Teixeira-Carvalho2
1Laboratório de Biologia das Interações Celulares, Departamento de Morfologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
Insights
In Chagas disease, higher CD86 expression on monocytes in asymptomatic patients correlates with regulatory T cells. This suggests a potential mechanism for immune regulation and controlling inflammation in indeterminate Chagas disease.
Area of Science:
- Immunology
- Infectious Diseases
- Parasitology
Background:
- Chagas disease presents an indeterminate (IND) asymptomatic form and a severe cardiac/digestive (CARD) form, with underlying mechanisms poorly understood.
- Monocyte and lymphocyte interactions, including co-stimulatory molecules CD80/CD86, are crucial for immune responses.
- Understanding monocyte subset profiles in Chagas disease is vital for elucidating disease progression.
Purpose of the Study:
- To characterize the functional-phenotypic profile of monocyte subsets in Chagas disease.
- To investigate the expression of co-stimulatory molecules (CD80, CD86) and other immune markers in IND and CARD patients.
- To explore the relationship between monocyte subsets and T lymphocyte activation in Chagas disease.
Main Methods:
- Flow cytometry was used to analyze monocyte subsets from IND, CARD, and non-infected (NI) individuals.
- Cells were stimulated *in vitro* with *Trypanosoma cruzi* antigens.
- Expression of CD80, CD86, TLR-2, TLR-4, TLR-9, HLA-DR, IL-10, IL-12, CTLA-4, and CD28 was assessed.
Main Results:
- Higher CD86 expression was observed on monocyte subsets in IND patients compared to NI individuals.
- IND patients showed a higher frequency of CD4+CTLA-4+ T lymphocytes after *T. cruzi* stimulation.
- Associations were found between CD80/CD28 and CD86/CTLA-4, with a high frequency of regulatory T (Treg) cells in IND patients.
Conclusions:
- CD86 may play a role in immunoregulation in asymptomatic Chagas disease through association with CTLA-4.
- The CD86-CTLA-4 interaction could influence Treg cell activation, potentially controlling inflammation and tissue damage.
- This study reveals novel insights into monocyte subset function in Chagas disease pathogenesis.
Abstract:
In the chronic phase of Chagas disease, 60% of the patients develop the asymptomatic form known as indeterminate (IND). The remaining 30% of the patients develop a life-threatening form in which digestive and/or cardiac (CARD) alterations take place. The mechanisms underlying the development of severe forms of Chagas disease remain poorly understood. It is well known that interactions between immune cells such as monocytes and lymphocytes drive immune responses. Further, the co-stimulatory molecules CD80 and CD86 expressed by monocytes and subsets induce lymphocyte activation, thereby triggering cellular immune response. Here, we revealed, for the first time, the functional-phenotypic profile of monocytes subsets in Chagas disease. Using flow cytometry, we evaluated the effect of in vitro stimulation with Trypanosoma cruzi antigens on the expression of the co-stimulatory molecules CD80 and CD86 in different monocyte subsets of patients with IND and CARD clinical forms of Chagas disease. We also assessed the expression of toll-like receptor (TLR)-2, TLR-4, TLR-9, HLA-DR, IL-10, and IL-12 in the monocyte subsets and of CTLA-4 and CD28, ligands of CD80 and CD86, in T lymphocytes. CD86 expression in all monocyte subsets was higher in IND patients when compared with non-infected (NI) individuals. After stimulation with T. cruzi, these patients also showed a higher frequency of CD4+CTLA-4+ T lymphocytes than NI individuals. We found an association between CD80 and CD28, and between CD86 and CTLA-4 expression, with a high frequency of regulatory T (Treg) cells in IND patients. We proposed that CD86 may be involved in immunoregulation by its association with CTLA-4 in asymptomatic patients. CD86 and CTLA-4 interaction may influence Treg activation, and this could represent a new strategy to control inflammation and tissue damage.
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