» Articles » PMID: 7706829

Immunochemotherapy for a Systemic Intracellular Infection: Accelerated Response Using Interferon-gamma in Visceral Leishmaniasis

Overview
Journal J Infect Dis
Date 1995 Apr 1
PMID 7706829
Citations 22
Authors
Affiliations
Soon will be listed here.
Abstract

To determine if cytokine immunotherapy accelerates the response to conventional treatment in visceral leishmaniasis (kala-azar), previously untreated Indian patients were given antimony for 30 days (n = 15) or antimony plus interferon-gamma (IFN-gamma; n = 16). After 10 days, 10 (63%) of 16 patients treated with antimony plus IFN-gamma versus 1 (7%) of 15 randomized to antimony alone were considered cured of parasites (P < .005). On day 20, 14 (93%) of 15 versus 6 (40%) of 15 patients, respectively, were apparent clinical cures (P < .006), and treatment was discontinued early in the 14 IFN-gamma treated responders. Day 30 apparent cure rates (100% vs. 73%) and 6-month ultimate cure responses (87% vs. 60%) were higher in IFN-gamma-treated patients but not statistically different from controls (P > .05). All 13 IFN-gamma-treated subjects who were cured (12 of whom received therapy for 20 days) have remained healthy with follow-up of 14-24 months (mean, 18.9). These results indicate that IFN-gamma successfully accelerates the parasitologic and clinical response to antimony treatment, an effect that should permit shortening the duration of conventional therapy in previously untreated kala-azar.

Citing Articles

Immunotherapy and immunochemotherapy in combating visceral leishmaniasis.

Yadagiri G, Singh A, Arora K, Mudavath S Front Med (Lausanne). 2023; 10:1096458.

PMID: 37265481 PMC: 10229823. DOI: 10.3389/fmed.2023.1096458.


Immunomodulatory Therapy of Visceral Leishmaniasis in Human Immunodeficiency Virus-Coinfected Patients.

Adriaensen W, Dorlo T, Vanham G, Kestens L, Kaye P, van Griensven J Front Immunol. 2018; 8:1943.

PMID: 29375567 PMC: 5770372. DOI: 10.3389/fimmu.2017.01943.


Immune Checkpoint Targets for Host-Directed Therapy to Prevent and Treat Leishmaniasis.

Kumar R, Bhushan Chauhan S, Ng S, Sundar S, Engwerda C Front Immunol. 2017; 8:1492.

PMID: 29167671 PMC: 5682306. DOI: 10.3389/fimmu.2017.01492.


Transcriptional Profiling in Experimental Visceral Leishmaniasis Reveals a Broad Splenic Inflammatory Environment that Conditions Macrophages toward a Disease-Promoting Phenotype.

Kong F, Saldarriaga O, Spratt H, Osorio E, Travi B, Luxon B PLoS Pathog. 2017; 13(1):e1006165.

PMID: 28141856 PMC: 5283737. DOI: 10.1371/journal.ppat.1006165.


PROBLEMS IN MANAGEMENT OF KALA AZAR: EXPERIENCE FROM BIHAR.

Rai S, Bandyopadhyay S Med J Armed Forces India. 2016; 57(2):117-9.

PMID: 27407312 PMC: 4925848. DOI: 10.1016/S0377-1237(01)80128-3.