Selected Publications

2024

Evaluation of genetic or cellular impairments in Type I IFN immunity in a cohort of young adults with critical COVID-19

Covill LE, Sendel A, Campbell TM, Piiroinen I, Lind Enoksson S, Wahren Borgström E, Hansen S, Ma K, Marits P, Norlin AC, Smith CIE, Kåhlin J, Eriksson LI, Bergman P, Bryceson YT

J Clin Immunol 2024 Jan; 44(50)

2023

Human skin-resident CD8+ T cells require RUNX2 and RUNX3 for induction of cytotoxicity and expression of the integrin CD49a

Zitti B, Hoffer E, Zheng W, Vinay Pandey R, Schlums H, Perinetti Casoni G, Fusi I, Nguyen L, Kärner J, Kokkinou E, Carrasco A, Gahm J, Ehrström M, Happaniemi S, Keita Å, Hedin C, Mjösberg J, Eidsmo L, Bryceson YT

Immunity 2023 Jun;56(6)

2022

Novel RAB27A variant associated with late-onset hemphagocytic lymphohistiocytosis alters effector protein binding

Zondag TCE, Torralba-Raga L, Van Laar JAM, Hermans MAW, Bouman A, Hollink IHIM, van Hagen PM, Briggs DA, Hume AN, Bryceson YT

J. Clin. Immunol. 2022 Nov;42(8)

Respiratory viral infections in otherwise healthy humans with inherited IRF7 deficiency

Campbell TM, Liu Z, Zhang Q, Moncada-Velez M, Covill LE, Zhang P, et al

J. Exp. Med. 2022 Jul 4;219(7)

2021

The transcription factor Bcl11b promotes both canonical and adaptive NK cell differentiation

Holmes TD, Vinay Pandey R, Helm EY, Schlums H, Han H, Campbell TM, et al

Sci. Immunol. 2021 Mar 12;6(57)

RhoG deficiency abrogates cytotoxicity of human lymphocytes and causes hemophagocytic lymphohistiocytosis

Kalinichenko A, Perinetti Casoni G, Dupre L, et al

Blood 2021 Jan 29;

2020

Alternative UNC13D Promoter Encodes a Functional Munc13-4 Isoform Predominantly Expressed in Lymphocytes and Platelets

Galgano D, Soheili T, Voss M, Torralba-Raga L, et al

Front Immunol. 2020 Jun 9;11:1154.

Diagnostic challenges for a novel SH2D1A mutation associated with X-linked lymphoproliferative disease. Torralba-Raga L, Tesi B, Chiang SCC, Schlums H, et al Pediatr Blood Cancer. 2020 Apr;67(4):e28184.

2019

IL2RB maintains immune harmony. Campbell TM, Bryceson YT J Exp Med. 2019 Jun 3;216(6):1231-1233.

Fatal Central Nervous System Lymphocytic Vasculitis after Treatment for Burkitt Lymphoma in a Patient with a SH2D1A Mutation. Neves JF, Raga LT, Chiang SCC, Tesi B, Vieira JP, Cordeiro AI, Borrego L, Bryceson YT. Pediatr Infect Dis J. 2019 Feb;38(2):e29-e31.

2018

Natural killer cells in inflammation and autoimmunity. Zitti B, Bryceson YT. Cytokine Growth Factor Rev. 2018 Aug;42:37-46.

HLH: genomics illuminates pathophysiological diversity. Tesi B, Bryceson YT. Blood. 2018 Jul 5;132(1):5-7. 

A RAB27A 5' untranslated region structural variant associated with late-onset hemophagocytic lymphohistiocytosis and normal pigmentation. Tesi B, Rascon J, Chiang SCC, Burnyte B, Löfstedt A, et al J Allergy Clin Immunol. 2018 Jul;142(1):317-321.e8.



2017

CD49a Expression Defines Tissue-Resident CD8+ T Cells Poised for Cytotoxic Function in Human Skin.
Cheuk S, Schlums H, Gallais Sérézal I, Martini E, Chiang SC, Marquardt N, et al
Immunity 2017 02;46(2):287-300

Adaptive NK cells can persist in patients with GATA2 mutation depleted of stem and progenitor cells.
Schlums H, Jung M, Han H, Theorell J, Bigley V, Chiang SC, et al
Blood 2017 04;129(14):1927-1939

Gain-of-function SAMD9L mutations cause a syndrome of cytopenia, immunodeficiency, MDS, and neurological symptoms.
Tesi B, Davidsson J, Voss M, Rahikkala E, Holmes TD, Chiang SCC, et al
Blood 2017 04;129(16):2266-2279

Acquired somatic mutations in PNH reveal long-term maintenance of adaptive NK cells independent of HSPCs.
Corat MA, Schlums H, Wu C, Theorell J, Espinoza DA, Sellers SE, et al
Blood 2017 04;129(14):1940-1946