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Carlos Rodriguez-Gallego

Explore the profile of Carlos Rodriguez-Gallego including associated specialties, affiliations and a list of published articles. Areas
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Articles 81
Citations 6226
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Recent Articles
1.
Abad M, Alerany C, Gonzalez L, Neth O, Payares-Herrera C, Rodriguez-Gallego C, et al.
Glob Reg Health Technol Assess . 2025 Jan; 12:9-15. PMID: 39882388
Background: Activated phosphoinositide 3-kinase (PI3K) δ Syndrome (APDS) is an ultra-rare, potentially life-threatening disease that lacks approved treatments in Spain. This study aimed to apply Multi-Criteria Decision Analysis (MCDA) to...
2.
Suarez-Pajes E, Marcelino-Rodriguez I, Hernandez Brito E, Gonzalez-Barbuzano S, Ramirez-Falcon M, Tosco-Herrera E, et al.
Respir Res . 2024 Oct; 25(1):374. PMID: 39415140
Background: Community-acquired pneumonia (CAP) is associated with high morbidity and hospitalization rate. In infectious diseases, host genetics plays a critical role in susceptibility and immune response, and the immune pathways...
3.
Abad M, Alerany C, Alsina L, Lopez Granados E, Neth O, Poveda J, et al.
Glob Reg Health Technol Assess . 2024 May; 11:124-130. PMID: 38784663
Introduction: Activated phosphoinositide 3-kinase (PI3K)δ syndrome (APDS) is an ultra-rare inborn error of immunity (IEI) combining immunodeficiency and immune dysregulation. This study determined what represents value in APDS in Spain...
4.
Garcia-Solis B, Tapia-Torres M, Garcia-Soidan A, Hernandez-Brito E, Martinez-Saavedra M, Lorenzo-Salazar J, et al.
J Allergy Clin Immunol . 2024 Apr; 154(3):819-826. PMID: 38579942
Background: Monoallelic loss-of-function IKZF1 (IKAROS) variants cause B-cell deficiency or combined immunodeficiency, whereas monoallelic gain-of-function (GOF) IKZF1 variants have recently been reported to cause hypergammaglobulinemia, abnormal plasma cell differentiation, autoimmune...
5.
Matuozzo D, Talouarn E, Marchal A, Zhang P, Manry J, Seeleuthner Y, et al.
Genome Med . 2024 Jan; 16(1):6. PMID: 38184654
No abstract available.
6.
Bastard P, Gervais A, Taniguchi M, Saare L, Sarekannu K, Le Voyer T, et al.
J Exp Med . 2024 Jan; 221(2). PMID: 38175961
We found that 19 (10.4%) of 183 unvaccinated children hospitalized for COVID-19 pneumonia had autoantibodies (auto-Abs) neutralizing type I IFNs (IFN-α2 in 10 patients: IFN-α2 only in three, IFN-α2 plus...
7.
Porte R, Silva-Gomes R, Theroude C, Parente R, Asgari F, Sironi M, et al.
Elife . 2023 May; 12. PMID: 37222419
is a major pathogen in children, elderly subjects, and immunodeficient patients. Pentraxin 3 (PTX3) is a fluid-phase pattern recognition molecule (PRM) involved in resistance to selected microbial agents and in...
8.
Matuozzo D, Talouarn E, Marchal A, Zhang P, Manry J, Seeleuthner Y, et al.
Genome Med . 2023 Apr; 15(1):22. PMID: 37020259
Background: We previously reported that impaired type I IFN activity, due to inborn errors of TLR3- and TLR7-dependent type I interferon (IFN) immunity or to autoantibodies against type I IFN,...
9.
Garcia-Garcia A, de Diego R, Flores C, Rinchai D, Sole-Violan J, Deya-Martinez A, et al.
J Exp Med . 2023 Mar; 220(5). PMID: 36880831
X-linked recessive deficiency of TLR7, a MyD88- and IRAK-4-dependent endosomal ssRNA sensor, impairs SARS-CoV-2 recognition and type I IFN production in plasmacytoid dendritic cells (pDCs), thereby underlying hypoxemic COVID-19 pneumonia...
10.
Lee D, Le Pen J, Yatim A, Dong B, Aquino Y, Ogishi M, et al.
Science . 2022 Dec; 379(6632):eabo3627. PMID: 36538032
Multisystem inflammatory syndrome in children (MIS-C) is a rare and severe condition that follows benign COVID-19. We report autosomal recessive deficiencies of , , or in five unrelated children with...