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Updated: May 6, 2026

New Tools to Expand Regulatory T Cells from HIV-1-infected Individuals
Published on: May 30, 2013
Expanding the scope of human immunology in the Journal of Human Immunity
Petter Brodin1,2,3, ,
1Department of Women's and Children's Health, Karolinska Institutet, Solna, Sweden.
Abstract:
The Journal of Human Immunity (JHI) publishes molecular, cellular, and clinical studies of patients with inborn errors of immunity, or their phenocopies, including autoimmune and somatic disorders. A central tenet in the field is that the current range of genetic immunological disorders is only the tip of the iceberg, given the wide range of conditions and populations, and countless patients not yet studied from this angle. Systematic research into causal monogenic lesions is appropriate and likely to be informative in many infectious, allergic, inflammatory, autoimmune, and malignant disorders. Rare or even private genetic etiologies may be of heuristic value, revealing physiological mechanisms disrupted by other, more common genetic or other causes in other patients. In this context, the journal welcomes all immunological studies in line with this vision, in which molecular, cellular, or clinical abnormalities in individuals are seen as candidate phenotypes, potentially driven by inborn errors of immunity-monogenic or otherwise-worthy of genetic investigation.
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