TY - JOUR
T1 - Increased levels of interleukin-10 and IgG3 are hallmarks of Indian Post-Kala-Azar Dermal Leishmaniasis
AU - Ganguly, Sudipto
AU - Das, Nilay Kanti
AU - Panja, Moumita
AU - Pal, Shekhar
AU - Modak, Dolanchampa
AU - Rahaman, Mehebubar
AU - Mallik, Sudeshna
AU - Guha, Subhashis Kamal
AU - Pramanik, Netai
AU - Goswami, Ramapada
AU - Barbhuiya, Joyashree Nath
AU - Saha, Bibhuti
AU - Chatterjee, Mitali
N1 - Funding Information:
Received 16 October 2007; accepted 8 January 2008; electronically published 29 April 2008. Potential conflicts of interest: none reported. Presented in part: 15th Annual Meeting of the International Cytokine Society, San Francisco, 26–30 October 2007 (abstract 41). Financial support: Council of Scientific and Industrial Research (grant CSIR/60/ 58/03-EMR II); University Grants Commission, Government of India (Senior Research Fellowship to S.G.). Reprints or correspondence: Dr. Mitali Chatterjee, Dept. of Pharmacology, Institute of Postgraduate Medical Education and Research, 244 B, Acharya JC Bose Rd., Kolkata 700 020, India ([email protected]).
PY - 2008/6/15
Y1 - 2008/6/15
N2 - Background. Post-kala-azar dermal leishmaniasis (PKDL), an established sequela of visceral leishmaniasis (VL), is proposed to facilitate anthroponotic transmission of VL, especially during interepidemic periods. Immunopathological mechanisms responsible for Indian PKDL are still poorly defined. Methods. Our study attempted to characterize the immune profiles of patients with PKDL or VL relative to that of healthy control subjects by immunophenotyping, intracellular cytokine staining of peripheral blood mononuclear cells, and enzyme-linked immunosorbent assay for serum cytokines and immunoglobulin G (IgG) subclasses. Results. Patients with PKDL had significantly raised percentages of peripheral CD3+CD8+ cells compared with control subjects, a difference that persisted after cure. Patients with PKDL showed an intact response to phytohemagglutinin, with the percentages of lymphocytes expressing interferon (IFN)-γ, interleukin (IL)-2, IL-4, and IL-10 being comparable to those in control subjects. Patients with VL had decreased IFN-γ and IL-2 expression, which was restored after cure, and increased IL-10 expression, which persisted after cure. In their response to Leishmania donovani antigen, patients with PKDL showed a 9.6-fold increase in the percentage of IL-10-expressing CD3+CD8+ lymphocytes compared with control subjects, and this percentage decreased with treatment. Patients with PKDL had raised levels of IgG3 and IgG1 (surrogate markers for IL-10), concomitant with increased serum levels of IL-10. Conclusions. IL-10 -producing CD3+CD8+ lymphocytes are important protagonists in the immunopathogenesis of Indian PKDL.
AB - Background. Post-kala-azar dermal leishmaniasis (PKDL), an established sequela of visceral leishmaniasis (VL), is proposed to facilitate anthroponotic transmission of VL, especially during interepidemic periods. Immunopathological mechanisms responsible for Indian PKDL are still poorly defined. Methods. Our study attempted to characterize the immune profiles of patients with PKDL or VL relative to that of healthy control subjects by immunophenotyping, intracellular cytokine staining of peripheral blood mononuclear cells, and enzyme-linked immunosorbent assay for serum cytokines and immunoglobulin G (IgG) subclasses. Results. Patients with PKDL had significantly raised percentages of peripheral CD3+CD8+ cells compared with control subjects, a difference that persisted after cure. Patients with PKDL showed an intact response to phytohemagglutinin, with the percentages of lymphocytes expressing interferon (IFN)-γ, interleukin (IL)-2, IL-4, and IL-10 being comparable to those in control subjects. Patients with VL had decreased IFN-γ and IL-2 expression, which was restored after cure, and increased IL-10 expression, which persisted after cure. In their response to Leishmania donovani antigen, patients with PKDL showed a 9.6-fold increase in the percentage of IL-10-expressing CD3+CD8+ lymphocytes compared with control subjects, and this percentage decreased with treatment. Patients with PKDL had raised levels of IgG3 and IgG1 (surrogate markers for IL-10), concomitant with increased serum levels of IL-10. Conclusions. IL-10 -producing CD3+CD8+ lymphocytes are important protagonists in the immunopathogenesis of Indian PKDL.
UR - http://www.scopus.com/inward/record.url?scp=46349093658&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=46349093658&partnerID=8YFLogxK
U2 - 10.1086/588387
DO - 10.1086/588387
M3 - Article
C2 - 18444882
AN - SCOPUS:46349093658
SN - 0022-1899
VL - 197
SP - 1762
EP - 1771
JO - Journal of Infectious Diseases
JF - Journal of Infectious Diseases
IS - 12
ER -