Ottavia M Delmonte
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Explore the profile of Ottavia M Delmonte including associated specialties, affiliations and a list of published articles.
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72
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3280
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Recent Articles
1.
Goetzke C, Massoud M, Frischbutter S, Guerra G, Ferreira-Gomes M, Heinrich F, et al.
Nature
. 2025 Mar;
PMID: 40074901
In a subset of children and adolescents, SARS-CoV-2 infection induces a severe acute hyperinflammatory shock termed multisystem inflammatory syndrome in children (MIS-C) at four to eight weeks after infection. MIS-C...
2.
Wachter B, Xu Q, Shi L, Burbelo P, Myint-Hpu K, Schwartzberg P, et al.
J Allergy Clin Immunol
. 2025 Mar;
PMID: 40044048
Background: Bivalent COVID-19 mRNA vaccines encoding Wuhan-1 and Omicron BA.4/5 spike proteins can prevent SARS-CoV-2 infection, but the quality of adaptive immune responses and the importance of hybrid immunity are...
3.
Nolan S, Vignali M, Klinger M, Dines J, Kaplan I, Svejnoha E, et al.
Front Immunol
. 2025 Mar;
16:1488851.
PMID: 40034696
We describe the establishment and current content of the ImmuneCODE™ database, which includes hundreds of millions of T-cell Receptor (TCR) sequences from over 1,400 subjects exposed to or infected with...
4.
Snyder T, Gittelman R, Klinger M, May D, Osborne E, Taniguchi R, et al.
Front Immunol
. 2025 Jan;
15():1488860.
PMID: 39840037
Introduction: T cells are involved in the early identification and clearance of viral infections and also support the development of antibodies by B cells. This central role for T cells...
5.
Bosticardo M, Dobbs K, Delmonte O, Martins A, Pala F, Kawai T, et al.
Sci Immunol
. 2025 Jan;
10(103):eadq1697.
PMID: 39792639
Human recombination-activating gene (RAG) deficiency can manifest with distinct clinical and immunological phenotypes. By applying a multiomics approach to a large group of -mutated patients, we aimed at characterizing the...
6.
Kuehn H, Bosticardo M, Arrieta A, Stoddard J, Pala F, Niemela J, et al.
J Allergy Clin Immunol
. 2024 Dec;
PMID: 39734035
Background: Heterozygous immunoproteasome 20 S subunit beta 10 (PSMB10) mutations can cause severe combined immunodeficiency and Omenn syndrome. Hematopoietic stem cell transplantation in these patients is associated with severe complications...
7.
Duran J, Sayed S, Dalalo M, Mauracher A, Knight M, Conrey P, et al.
bioRxiv
. 2024 Dec;
PMID: 39713308
Signal transduction downstream of activating stimuli controls CD8+ T cell biology, however these external inputs can become uncoupled from transcriptional regulation in Primary Immune Regulatory Disorders (PIRDs). Gain-of-function (GOF) variants...
8.
Gall A, Bosticardo M, Ma S, Chen K, Amini K, Pala F, et al.
Front Immunol
. 2024 Oct;
15:1438383.
PMID: 39364398
Pathogenic variants in the transcription factor are associated with clinically overlapping syndromes including ectrodactyly-ectodermal dysplasia clefting (EEC) and ankyloblepharon-ectodermal defects-cleft lip/palate (AEC). T cell lymphopenia has rarely been described in...
9.
Arango-Franco C, Ogishi M, Unger S, Delmonte O, Orrego J, Yatim A, et al.
J Clin Invest
. 2024 Oct;
134(19).
PMID: 39352394
Infants with biallelic IL7R loss-of-function variants have severe combined immune deficiency (SCID) characterized by the absence of autologous T lymphocytes, but normal counts of circulating B and NK cells (T-B+NK+...
10.
Molitor A, Lederle A, Radosavljevic M, Sapuru V, Zavorka Thomas M, Yang J, et al.
Sci Adv
. 2024 Sep;
10(37):eado5545.
PMID: 39270020
Inositol 1,4,5-trisphosphate (IP3) receptor type 1 (), (), and () encode the IP3 receptor (IP3R), a key player in intracellular calcium release. In four unrelated patients, we report that an...