日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Humoral and cell-mediated immune responses to COVID-19 vaccines up to 6 months post three-dose primary series in adults with inborn errors of immunity and their breakthrough infections

在患有先天性免疫缺陷的成年人中,完成三剂次新冠疫苗基础免疫接种后长达 6 个月内,体液和细胞介导的免疫反应及其突破性感染情况。

Unninayar, Dana; Falcone, Emilia L; Chapdelaine, Hugo; Vinh, Donald C; Top, Karina A; Derfalvi, Beata; Issekutz, Thomas B; Decaluwe, Hélène; Pham-Huy, Anne; Upton, Julia; Betschel, Stephen D; Rubin, Tamar; Suresh, Sneha; Wright, Nicola A M; Murguía-Favela, Luis; Kalashnikova, Tatiana; Barrett, Lisa; Oldford, Sharon; Langlois, Marc-Andre; Arnold, Corey; Sadarangani, Manish; Zhang, Tinghua; Ramsay, Tim; Yazji, Dina; Cowan, Juthaporn

Differences in IDO1(+) dendritic cells and soluble CTLA-4 are associated with differential clinical responses to methotrexate treatment in rheumatoid arthritis

IDO1(+)树突状细胞和可溶性CTLA-4的差异与类风湿性关节炎患者对甲氨蝶呤治疗的不同临床反应相关

Malik, Anikó E; Slauenwhite, Drew; McAlpine, Sarah M; Hanly, John G; Marshall, Jean S; Issekutz, Thomas B

Differential type I and type III interferon expression profiles in rheumatoid and juvenile idiopathic arthritis

类风湿性关节炎和幼年特发性关节炎中I型和III型干扰素表达谱的差异

Malik, Anikó E; Slauenwhite, Drew; McAlpine, Sarah M; Hanly, John G; Marshall, Jean S; Dérfalvi, Beáta; Issekutz, Thomas B

Prolidase deficiency, a rare inborn error of immunity, clinical phenotypes, immunological features, and proposed treatments in twins

脯氨酸酶缺乏症,一种罕见的先天性免疫缺陷,双胞胎的临床表型、免疫学特征及拟议治疗方案

Alrumayyan, Nora; Slauenwhite, Drew; McAlpine, Sarah M; Roberts, Sarah; Issekutz, Thomas B; Huber, Adam M; Liu, Zaiping; Derfalvi, Beata

High Dose Intravenous IgG Therapy Modulates Multiple NK Cell and T Cell Functions in Patients With Immune Dysregulation

高剂量静脉注射IgG疗法可调节免疫失调患者的多种NK细胞和T细胞功能

McAlpine, Sarah M; Roberts, Sarah E; Heath, John J; Käsermann, Fabian; Issekutz, Andrew C; Issekutz, Thomas B; Derfalvi, Beata

Toll-like receptor 2 activation induces C-C chemokine receptor 2-dependent natural killer cell recruitment to the peritoneum

Toll 样受体 2 激活诱导 CC 趋化因子受体 2 依赖性自然杀伤细胞募集至腹膜

Ian D Haidl, Dihia Meghnem, Thomas B Issekutz, Jean S Marshall

IPEX Syndrome with Normal FOXP3 Protein Expression in Treg Cells in an Infant Presenting with Intractable Diarrhea as a Single Symptom

IPEX综合征伴Treg细胞中FOXP3蛋白表达正常,患儿仅表现为顽固性腹泻这一单一症状

Al Maawali, Ali; Derfalvi, Beata; Van Limbergen, Johan; Issekutz, Andrew; Issekutz, Thomas; Ghandourah, Hasan; Rashid, Mohsin

Differential regulation of Ca(2+) influx by ORAI channels mediates enamel mineralization

ORAI通道对Ca(2+)内流的差异性调节介导牙釉质矿化

Eckstein, Miriam; Vaeth, Martin; Aulestia, Francisco J; Costiniti, Veronica; Kassam, Serena N; Bromage, Timothy G; Pedersen, Pal; Issekutz, Thomas; Idaghdour, Youssef; Moursi, Amr M; Feske, Stefan; Lacruz, Rodrigo S

T-cell defects in patients with ARPC1B germline mutations account for combined immunodeficiency

ARPC1B 生殖系突变患者的 T 细胞缺陷是导致联合免疫缺陷的原因。

Brigida, Immacolata; Zoccolillo, Matteo; Cicalese, Maria Pia; Pfajfer, Laurène; Barzaghi, Federica; Scala, Serena; Oleaga-Quintas, Carmen; Álvarez-Álvarez, Jesus A; Sereni, Lucia; Giannelli, Stefania; Sartirana, Claudia; Dionisio, Francesca; Pavesi, Luca; Benavides-Nieto, Marta; Basso-Ricci, Luca; Capasso, Paola; Mazzi, Benedetta; Rosain, Jeremie; Marcus, Nufar; Lee, Yu Nee; Somech, Raz; Degano, Massimo; Raiola, Giuseppe; Caorsi, Roberta; Picco, Paolo; Moncada Velez, Marcela; Khourieh, Joelle; Arias, Andrés Augusto; Bousfiha, Aziz; Issekutz, Thomas; Issekutz, Andrew; Boisson, Bertrand; Dobbs, Kerry; Villa, Anna; Lombardo, Angelo; Neven, Benedicte; Moshous, Despina; Casanova, Jean-Laurent; Franco, José Luis; Notarangelo, Luigi D; Scielzo, Cristina; Volpi, Stefano; Dupré, Loïc; Bustamante, Jacinta; Gattorno, Marco; Aiuti, Alessandro

ORAI1 mutations abolishing store-operated Ca(2+) entry cause anhidrotic ectodermal dysplasia with immunodeficiency

ORAI1 基因突变导致储存操纵型 Ca(2+) 内流消失,从而引起无汗型外胚层发育不良伴免疫缺陷。

Lian, Jayson; Cuk, Mario; Kahlfuss, Sascha; Kozhaya, Lina; Vaeth, Martin; Rieux-Laucat, Frédéric; Picard, Capucine; Benson, Melina J; Jakovcevic, Antonia; Bilic, Karmen; Martinac, Iva; Stathopulos, Peter; Kacskovics, Imre; Vraetz, Thomas; Speckmann, Carsten; Ehl, Stephan; Issekutz, Thomas; Unutmaz, Derya; Feske, Stefan