Add BrightSurf on Google Email

The catch 22 of immune response to AIDs viral infection

A recent study by Mark Feinberg and colleagues reveals that the level of immune activation directly affects the initial peak of virus in the blood stream. The researchers also found that steady-state viral levels in chronic infection are related to the generation of a primary immune response, which may be both helpful and harmful.

SourceJCI Journals·JournalJournal of Clinical Investigation·DateMar 15, 2004

Viral immunosuppression: Not just a game of hide and go seek

Researchers have identified a dual strategy used by viruses to subvert the immune system, involving the targeting of hematopoietic progenitors and inhibition of dendritic cell maturation. This study sheds light on the mechanisms of viral immunosuppression, enabling better understanding of immune evasion tactics.

SourceJCI Journals·JournalJournal of Clinical Investigation·DateMar 1, 2004

Understanding the autoimmune response in type 1 diabetes

Researchers developed a novel assay to examine T cell responses to autoantigens in islet cells, revealing distinct pathways of T cell differentiation and maturation in normal individuals versus patients with T1DM. These findings suggest proinflammatory polarization in diabetes but regulatory phenotypes in health.

SourceJCI Journals·JournalJournal of Clinical Investigation·DateFeb 2, 2004

JCI table of contents, February 2, 2004

A novel assay reveals that T cells in patients with type 1 diabetes produce pro-inflammatory cytokines, driving an autoaggressive immune response. In contrast, healthy individuals' T cells produce regulatory cytokines, maintaining tolerance. The findings offer new approaches to immune modulation and tolerance.

SourceJCI Journals·JournalJournal of Clinical Investigation·DateFeb 2, 2004

Turning foe into friend with lentiviral vectors

Researchers have developed a third-generation lentivector that transduces dendritic cells in vivo, inducing a strong and persistent antigen-specific immune response. This approach may replace costly and labor-intensive methods currently used to elicit tumor-specific cytotoxic T lymphocyte responses.

SourceJCI Journals·JournalJournal of Clinical Investigation·DateJun 2, 2003