Related Experiment Videos
Immunosuppression in Kenyan visceral leishmaniasis
Clinical and Experimental Immunology
|February 1, 1983
Summary
Visceral leishmaniasis in Kenya causes significant immunosuppression, affecting both specific and non-specific immune responses. Some patients remain unresponsive to leishmanial antigens even after treatment.
Area of Science:
- Immunology
- Infectious Diseases
- Tropical Medicine
Background:
- Visceral leishmaniasis is an endemic parasitic disease in Kenya.
- Cell-mediated immunity plays a crucial role in controlling leishmaniasis.
- Understanding immune responses is vital for managing the disease.
Purpose of the Study:
- To evaluate cell-mediated immune responses in Kenyan patients with active visceral leishmaniasis.
- To assess both in vivo and in vitro immune reactions to various antigens and mitogens.
- To investigate the nature and extent of immunosuppression in visceral leishmaniasis.
Main Methods:
- Skin testing with leishmanin, tuberculin, streptococcal, and candida antigens in patients and controls.
- In vitro lymphocyte blastogenic transformation assays using phytohaemagglutinin (PHA), concanavalin A (Con A), purified protein derivative (PPD), streptokinase-streptodornase (SKSD), and leishmanial antigen (LA).
- Comparison of immune responses between patients with active visceral leishmaniasis and age/sex-matched controls.
Main Results:
- The majority of patients exhibited complete anergy (unresponsiveness) to all tested antigens both in vivo and in vitro.
- Suppression of lymphocyte responses to non-specific mitogens (PHA, Con A) was less pronounced than to specific antigens.
- Recovery of non-specific immune responses was observed to precede the development of specific immunity.
- A subset of patients (23%) showed persistent immune unresponsiveness to leishmanial antigens one year post-treatment.
Conclusions:
- Visceral leishmaniasis in Kenya is associated with profound specific and non-specific immunosuppression.
- Immune recovery is a gradual process, with non-specific responses often returning before specific immunity.
- Persistent immune unresponsiveness post-cure highlights potential challenges in complete disease resolution and relapse prevention.