TY - JOUR
T1 - Expanding the scope of human immunology in the Journal of Human Immunity
AU - JHI associate consulting editors
AU - JHI society editors
AU - Brodin, Petter
AU - Cooper, Megan
AU - Casanova, Jean Laurent
AU - Bogunovic, Dusan
AU - Gennery, Andy
AU - Hsieh, Elena
AU - Meyts, Isabelle
AU - Morio, Tomohiro
AU - Poli, Cecilia
AU - Puel, Anne
AU - Romberg, Neil
AU - Sankaran, Vijay
AU - Su, Helen
AU - Tangye, Stuart
AU - Turvey, Stuart
AU - Zhang, Shen Ying
AU - Crow, Yanick
AU - Milner, Josh
AU - Notarangelo, Luigi
AU - Aggarwal, Amita
AU - Al-Mousa, Hamoud
AU - Bousfiha, Ahmed Aziz
AU - Hambleton, Sophie
AU - Hauck, Fabian
AU - Lucas, Carrie L.
AU - Ma, Cindy S.
AU - Naumova, Elissaveta
AU - Okada, Satoshi
AU - Prando, Carolina
AU - Rawat, Amit
AU - Rezaei, Nima
AU - Snow, Andrew L.
AU - Wang, Xiaochuan
N1 - Publisher Copyright:
© 2026 Brodin et al.
PY - 2026/3/2
Y1 - 2026/3/2
N2 - 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.
AB - 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.
UR - https://www.scopus.com/pages/publications/105039264863
U2 - 10.70962/jhi.20260012
DO - 10.70962/jhi.20260012
M3 - Editorial
AN - SCOPUS:105039264863
SN - 3065-8993
VL - 2
JO - Journal of Human Immunity
JF - Journal of Human Immunity
IS - 2
M1 - e20260012
ER -