Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 1982 Jul-Aug;4(4):756-62.
doi: 10.1093/4.4.756.

Immune responses in parasitic diseases. Part B: mechanisms

Review

Immune responses in parasitic diseases. Part B: mechanisms

R K Chandra. Rev Infect Dis. 1982 Jul-Aug.

Abstract

A number of host defenses provide variable resistance against parasites. From the biological point of view, invading parasites must not eliminate the susceptible host population; therefore, antiparasite immunity plays an essential role in limiting the invasion and proliferation of parasites. Several differences exist between immune responses to parasites and immune responses to other microorganisms. Effector mechanisms include T lymphocyte-mediated inflammatory granuloma formation and encapsulation involving the deposition of fibrous tissue. In some instances, passive immunity can be transferred by serum antibodies. Antibodies may act via complement fixation, granulocyte adhesion, opsonization, inhibition of invasion, or mast cell degranulation. Of the nonspecific factors, macrophage activation, natural killer cells, and serum factors other than antibodies are critical in the battle against parasites. The net result of these immune responses may be antiparasitic, proparasitic, of no consequence to either host or parasite, or harmful to the host.

PubMed Disclaimer

LinkOut - more resources