Clinical Immunology

Papers
(The TQCC of Clinical Immunology is 5. The table below lists those papers that are above that threshold based on CrossRef citation counts [max. 250 papers]. The publications cover those that have been published in the past four years, i.e., from 2021-04-01 to 2025-04-01.)
ArticleCitations
5-HT is associated with the dysfunction of regulating T cells in patients with allergic rhinitis166
Retraction notice to “Prevention of carrageenan-induced pleurisy in mice by anti-CD30 ligand monoclonal antibody” [Clin. Immunol. 113/1 (2004) 64–73]144
Complement C5a and C5a receptor 1 mediates glomerular damage in focal segmental glomerulosclerosis91
Intima-media thickness of common femoral vein is increased in Behçet's disease90
Positive rates of interferon-γ release assay and tuberculin skin test in detection of latent tuberculosis infection: A systematic review and meta-analysis of 200,000 head-to-head comparative tests74
Difficult-to-treat Behçet syndrome: A therapeutic approach60
Lymphocyte alterations in patients with Common Variable Immunodeficiency (CVID) and autoimmune manifestations56
Roles of prostaglandins in immunosuppression55
IL-27 promotes pathogenic T cells in a mouse model of Sjögren's disease48
A bispecific antibody targeting HLA-DQ2.5-gluten peptides potently blocks gluten-specific T cells induced by gluten ingestion in patients with celiac disease47
Immune reconstitution and survival, following hematopoietic stem cell transplantation in Omani patients with inborn errors of immunity46
Earlier and more aggressive treatment with biologics may prevent relapses and further new organ involvement in Behçet's disease46
CD36 regulates macrophage and endothelial cell activation and multinucleate giant cell formation in anti neutrophil cytoplasm antibody vasculitis45
Age-dependent transcriptomic profiles of leukocytes in pediatric population41
Integration of metalloproteome and immunoproteome reveals a tight link of iron-related proteins with COVID-19 pathogenesis and immunity40
Autosomal recessive T-bet and RORgammaT deficiencies underlie mycobacterial susceptibility38
Editorial Board38
Association of SARS-COV-2 viral RNAemia, IL- 6 gene polymorphism, serum IL-6 and peripheral blood lymphocytes and monocytes with disease severity in COVID-19 patients37
Predominant Antibody Deficiency and Risk of Microscopic Colitis: A Nationwide Case-Control Study in Sweden36
Behçet's patients' response to COVID-19 vaccination36
Diagnostic significance of TREC and KRE Cevaluation in case of primary immunodeficiencies36
Editorial Board36
Opportunities for diagnostics of congenital and acquired immunological disorders in the Republic of Belarus35
Impact of Early Intervention for STAT3 Dominant-Negative Disease35
Effectiveness of T2 biologics in patients with common variable immune deficiency and allergic respiratory disease33
Response to Tofacitinib in an Infant with Aicardi-Goutières Syndrome due to Biallelic Variants in RNU7–133
GATA2 at 10: Emergence of Genotype-Phenotye correlations32
Challenges of Diagnostic Approach in a Hyper-IgE Syndrome Family31
Epstein Barr Virus Positive Hodgkin's Lymphoma in a Patient with NEMO Deficiency31
Characterizing A Novel Variant in ABCB1 in a Family with Activated PI3K Delta Syndrome-like Presentation30
B-cell driven autoimmunity in two patients with monogenic autoinflammatory disorders30
IgG Replacement Therapy Use in Patients with Hypogammaglobulinemia after Lung Transplant30
Expandig Lentiviral Vectors cargo capacity with protein trans-splicing29
A Rare Immunodeficiency As a Cause of Inflammatory Bowel Disease; ARPC1B Deficiency28
Characterization of Adaptive Immune Responses to SARS-CoV-2 Updated Bivalent Booster28
Temporal viral loads in respiratory and gastrointestinal tract and serum antibody responses during SARS-CoV-2 infection in an Italian pediatric cohort27
Patterns of IgG Testing and Rates of Hypogammaglobulinemia in Patients With Chronic Lymphocytic Leukemia or Small Lymphocytic Lymphoma27
Diabetes mellitus aggravates humoral immune response in myasthenia gravis by promoting differentiation and activation of circulating Tfh cells27
Editorial Board26
Toll-like receptor 10 expression in B cells is negatively correlated with the progression of primary Sjögren's disease26
Cyclic helix B peptide ameliorated the sepsis-induced injury in human HPMEC cells through regulating NF-κB26
Lack of DOCK8 impairs the primary biologic functions of human NK cells and abrogates CCR7 surface expression in a WASP-independent manner26
Could Osteopontin be a useful biomarker in the diagnosis and severity assessment of osteoarthritis? A systematic review and meta-analysis of recent evidence26
Systematic analyses to explore immune gene sets-based signature in hepatocellular carcinoma, in which IGF2BP3 contributes to tumor progression25
BCL10 loss-of-function novel mutation leading to atypical severe combined immunodeficiency25
Dok-1 regulates mast cell degranulation negatively through inhibiting calcium-dependent F-actin disassembly25
The possible involvement of sema3A and sema4A in the pathogenesis of multiple sclerosis25
Editorial Board24
Exploring the role of insulin-like growth factor binding protein-1 in identifying idiopathic multicentric Castleman's disease types: Implications for the mTOR signaling pathway24
Alterations in the innate and adaptive immune system in a real-world cohort of multiple sclerosis patients treated with ocrelizumab24
Editorial Board24
Biallelic MTHFD1 variants presenting as severe combined immunodeficiency24
Muller morphs redefined by a multimorphic IRF4 variant presenting as CID with PCP susceptibility23
Racial and Ethnic Disparities in Outcomes following Hematopoietic Stem Cell Transplant (HCT) in Patients with Severe Combined Immunodeficiency (SCID)23
Contents23
AIOLOS haploinsufficiency is associated with immunodeficiency, autoimmunity, and allergy23
Publication Information23
MMF-Driven Disruption of B-cell Populations as a Biomarker for Infection Risk in Solid Organ Transplant Recipients22
Gut immunopathological signatures in Rag1 hypomorphic mice22
RAC2 mutations and immune deficiency – functional spectrum of an international cohort22
Myocarditis in a congenital STAT1 gain-of-function patient21
IFIH1 deficiency causing neonatal herpes simplex virus encephalitis and recurrent retinitis21
High rate of molecular diagnosis among individuals with alopecia with known or suspected inborn errors of immunity21
Mild COVID-19 outcomes in adults with inborn errors of immunity: a single-center experience21
Assessment of disease activity and management of patients with NFkB1 insufficiency21
Long-term safety of facilitated subcutaneous immunoglobulin 10% treatment in patients with primary immunodeficiency diseases: final analysis from a post-authorization safety study conducted in the USA20
Molecular profile of patients with inborn errors of immunity from Nepal20
Variants detection in regions of segmental duplication facilitates molecular diagnosis for IEI such as chronic granulomatous disease caused by NCF1 mutations20
Mild COVID-19 clinical course among paediatric patients with primary immunodeficiency20
Use of Dupilumab in HyperIgE syndrome with ERBIN-deficiency: case report20
An Unreported homozygous variant within Lipopolysaccharide responsive beige-like anchor (LRBA) gene in a child exhibiting with infantile type 1 diabetes mellitus19
Prevalence of Increased Hepatic Stiffness and Fat Fraction in STAT3 Dominant Negative Disease19
Correlation between levels of anti-cytokine antibodies, recombination activity of the mutant RAG proteins and clinical phenotype in patients with RAG deficiency19
Family History of Agammaglobulinemia Among Racial and Ethnic Minority Groups with X-linked Agammaglobulinemia from the USIDNET Registry19
The Use of Novel Antibodies to Characterize B cells in Health and Disease19
Lupus nephritis with clinical and laboratory features of humoral immune deficiency in a 29-year-old female with a novel NCF1 variant consistent with autosomal recessive chronic granulomatous disease18
Primary immunodeficiency associated with a SAMD9L mutation18
A Case of X-Linked Moesin-Associated Immune Deficiency in a Pediatric Patient18
Dupilumab as Adjunct Treatment for Persistent Food Allergy in Adulthood18
Distinct Patterns in Treg and T-helper Subset Reconstitution After Autologous Hematopoietic Stem Cell Transplantation in Juvenile-onset Systemic Sclerosis Patients18
A report on the clinical efficacy of rituximab administration in patients with inborn errors of immunity and autoimmune manifestations18
Hypomorphic splice site IL2RG variants associated with Cryptosporidium liver disease18
Maternal Health Characteristics Associated with Idiopathic T Cell Lymphopenia of Infancy18
Multiple Intestinal Atresia with Combined Immunodeficiency, a New Gene Arises18
Curious cases of GATA2 deficiency: clonal evolution or dual diagnoses?18
108 PU.1-associated inborn errors of immunity: new mutations, phenotypes, and inheritance patterns17
Treatment of B-cell depleted COVID-19 patients with convalescent plasma and plasma-based products17
126 Use of ruxolitinib for patients with hyperinflammatory syndromes – a real-world experience pilot study17
167 Differentiating IPEX- like syndrome from other causes of autoimmune enteropathy17
RIP2-deficiency induces inflammation in response to SV40 Large T induced genotoxic stress through altered ROS homeostasis17
2 Maternal and neonate outcomes following exposure to hyaluronidase-facilitated subcutaneous immunoglobulin 10% during pregnancy: a retrospective case series based on US claims data17
59 Comparison of quality improvement programs relevant in next-generation sequence data analysis17
Editorial Board17
TET2-mediated upregulation of 5-hydroxymethylcytosine in LRRC39 promoter promotes Th1 response in association with downregulated Treg response in Vogt-Koyanagi-Harada disease17
208 A Subtle Clinical Presentation of LAD1 Deficiency16
87 Phenotypic variability of Circulating Natural Killer Cells in healthy donors16
49 Early-Onset Common Variable Immunodeficiency in a Patient with Heterozygous Variants in Interferon Response-Associated Genes TRAF3 and IRF416
17 Severe Cardiac Tamponade in an Unusual Case of CTLA-4 Haploinsufficiency16
116 Relative location of prime-boost immunization determines memory B cell fate16
206 Oral Pathology in STAT3DN Hyper IgE Syndrome16
71 Two allelic variants in the SERPING1 gene associated with hereditary angioedema detected in one adult patient without clinical manifestation of the disease. Case report16
29 Safety and feasibility of the use of dual cardiac-thymus transplant in a child with cardiac failure requiring heart transplant16
146 Transient severe T cell lymphopenia in a patient with Cornelia de Lange Syndrome captured by TREC screening16
176 JAK1-selective inhibitor upadacitinib induced dynamic immunologic alterations and clinical response in treatment-resistant CVID gastrointestinal disease15
57 Development and Implementation of the TRIO Health Activated Phosphoinositide 3-kinase Delta Syndrome Characterization and Clinical Outcomes Immunologic Registry (APDS-CHOIR)15
195 DHR-based Flow Cytometry Beyond CGD15
166 PRF1-Related Isolated CNS Hemophagocytic Lymphohistiocytosis Successfully Treated with Ruxolitinib Monotherapy15
173 Spatial mapping of immune cells in barrier tissues of immunocompromised patients affected by human papillomavirusrelated disease15
19 POLD3 deficiency is associated with syndromic severe combined immunodeficiency including neurodevelopmental delay and hearing impairment15
191 CMV-specific adaptive immune response in U.S. Mennonite patients with hypomorphic RAG1 or RAG2 mutations presenting with clinical variability15
194 Characterizing a unique B-cell precursor population as a potential diagnostic tool for WHIM syndrome and APDS15
122 A Quantitative Approach for Identifying Health Disparities Driving Diagnostic and Treatment Delays in VEO-IBD15
164 Enteropathy in Patients with Common Variable Immunodeficiency: A Dutch Cohort Study15
51 Polymicrobial necrotizing pneumonia in a 3-year-old child with nearabsent pneumococcal antibody and mitogen interferon-γ responses14
140 Late Onset and Long Lasting Neutropenias: preliminary data on WES analysis14
AXL+SIGLEC6+ dendritic cells in cerebrospinal fluid and brain tissues of patients with autoimmune inflammatory demyelinating disease of CNS14
16 Bone marrow damage in patients with Adenosine Deaminase 2 Deficiency14
95 Patterns and presentations of mosaic variation in monogenic acquired errors of immunity14
94 Compound heterozygous mutations in the kinase domain of IKKα lead to immunodeficiency and immune dysregulation14
101 Predictive Model for Aiding in Early Common Variable Immunodeficiency Diagnosis14
161 Human ITCH E3 Ubiquitin Protein Ligase (ITCH) Deficiency Syndrome Successfully Treated with Hematopoietic Cell Transplant (HCT)14
142 A non-consanguineous family with hepatic veno-occlusive disease and immunodeficiency14
117 Clinical and Immunologic Phenotype of Prolidase Deficiency14
150 From pancytopenia to hyperleukocytosis, an unexpected presentation of immune reconstitution inflammatory syndrome in an infant with methylmalonic acidemia14
Evidence that platelets from transfusion-dependent β-thalassemia patients induce T cell activation13
Distinct NOD2 mutations reported in three families with Blau syndrome (BS) from a single center in India - Case series and review of literature13
Citrullination: A modification important in the pathogenesis of autoimmune diseases13
Transcriptomic and proteomic profiling reveals distinct pathogenic features of peripheral non-classical monocytes in systemic lupus erythematosus13
Two cases of pediatric primary immunodeficiency caused by a familial moesin(MSN)gene mutation13
Distinct innate and adaptive immunity phenotypic profile at the circulating single-cell level in Psoriatic Arthritis13
Interrelation of T cell cytokines and autoantibodies in systemic lupus erythematosus: A cross-sectional study13
Infection with SARS-CoV-2 primes immunological memory in human nasal-associated lymphoid tissue13
Tyro3 receptor tyrosine kinase contributes to pathogenic phenotypes of fibroblast-like synoviocytes in rheumatoid arthritis and disturbs immune cell balance in experimental arthritis13
Lessons learned from the diagnostic work-up of a patient with the bare lymphocyte syndrome type II13
Increased CYR61 expression activates CCND1/c-Myc pathway to promote nasal epithelial cells proliferation in chronic rhinosinusitis with nasal polyps13
Determining reference ranges for lymphocyte proliferation responses to phytohemagglutinin and Bacillus Calmette–Guérin in Iranian children13
Longitudinal analysis of urinary proteins in lupus nephritis – A pilot study13
Advantages of plasmatic CXCL-10 as a prognostic and diagnostic biomarker for the risk of rejection and subclinical rejection in kidney transplantation12
Antibody and T-cellular response to COVID-19 booster vaccine in SARS-CoV-1 survivors12
TNF-inhibitors or bisphosphonates in chronic nonbacterial osteomyelitis? - Results of an international retrospective multicenter study12
AIM2 inflammasome: A potential therapeutic target in ischemic stroke12
The platelet-mitochondria nexus in autoimmune and musculoskeletal diseases12
Combined spinal-epidural anesthesia with acupoint injection for labor anesthesia reduces IL-1β/IL-10 ratio in maternal peripheral blood, umbilical cord blood and improves the labor outcomes: A prospec12
Cellular changes in eculizumab early responders with generalized myasthenia gravis12
Association between systemic lupus erythematosus and myasthenia gravis: A population-based National Study12
Editorial Board12
Epigenetic regulation of T cell lineages in skin and blood following hematopoietic stem cell transplantation12
Early prediction of COVID-19 outcome using artificial intelligence techniques and only five laboratory indices12
Retroviral glycoprotein-mediated immune suppression via the potassium channel KCa3.1 – A new strategy for amelioration of inflammatory bowel diseases12
Epidemiology of combined immunodeficiencies affecting cellular and humoral immunity– a multicentric retrospective cohort study from the Arabian Peninsula12
SARS-CoV-2/COVID-19 and its relationship with NOD2 and ubiquitination12
Efficacy and safety of tripterygium wilfordii Hook F plus TNF inhibitor for active rheumatoid arthritis: A multicentre, randomized, double-blind, triple-dummy controlled trial12
NLRP12-associated autoinflammatory disease: A novel causal mutation and bioinformatics analyses12
Deep immune profiling of chronic rhinosinusitis in allergic and non-allergic cohorts using mass cytometry12
A nomogram to predict the risk of proliferative lupus nephritis in patients with systemic lupus erythematosus involving the kidneys12
Role of soluble epoxide hydrolase in the abnormal activation of fibroblast-like synoviocytes from patients with rheumatoid arthritis11
Advancements in the characterization of tissue resident memory T cells in skin disease11
Effect of DNA methylation at the CTLA4 gene on the clinical status of autoimmune thyroid diseases11
DOCK8 deficiency due to a deep intronic variant in two kindreds with hyper-IgE syndrome11
Aberrant monocyte subsets in patients with Behçet's disease11
Differential contributions of the C5b-9 and C5a/C5aR pathways to microvascular and macrovascular thrombosis in complement-mediated thrombotic microangiopathy patients11
Bruton's tyrosine kinase ablation inhibits B cell responses and antibody production for the prevention of chronic rejection in cardiac transplantation11
Myxomavirus serpin alters macrophage function and prevents diffuse alveolar hemorrhage in pristane-induced lupus11
Neuroimmunology: PIK3R1 Ile571TyrfsTer31 plays an important role in neuronal function and survival11
Prolonged diagnostic journey in delayed-onset adenosine deaminase deficiency11
Aberrant tolerogenic functions and proinflammatory skew of dendritic cells in STAT1 gain-of-function patients may contribute to autoimmunity and fungal susceptibility11
Presence of ectopic germinal center structures in autoimmune hepatitis11
Immunological features of circulating monocyte subsets in patients with squamous cell carcinoma of the head and neck11
Changes in immune function and immunomodulatory treatments of septic patients11
Bone marrow CD8+ Trm cells induced by IL-15 and CD16+ monocytes contribute to HSPC destruction in human severe aplastic anemia11
Mechanisms of age-related Treg dysfunction in an arthritic environment11
CXCL-8 as a signature of severe Helicobacter pylori infection and a stimulator of stomach region-dependent immune response10
Identification of signature of tumor-infiltrating CD8 T lymphocytes in prognosis and immunotherapy of colon cancer by machine learning10
Dynamics of HIV reservoir decay and naïve CD4 T-cell recovery between immune non-responders and complete responders on long-term antiretroviral treatment10
Ionic reverberation modulates the cellular fate of CD8+tissue resident memory T cells (TRMs) in patients with renal cell carcinoma: A novel mechanism10
Large deletion in 6q containing the TNFAIP3 gene associated with autoimmune lymphoproliferative syndrome10
Novel insight into MDA-7/IL-24: A potent therapeutic target for autoimmune and inflammatory diseases10
Gut dysbiosis and multiple sclerosis10
COVID-19 in children and young adults with moderate/severe inborn errors of immunity in a high burden area in pre-vaccine era10
Age-dependent decrease of circulating T follicular helper cells correlates with disease severity in elderly patients with COVID-1910
Dysregulation of neutrophil extracellular traps (NETs)-related genes in the pathogenesis of diabetic kidney disease - Results from bioinformatics analysis and translational studies10
A Disintegrin and metalloproteinase carves T cell abnormalities and pathogenesis in systemic lupus erythematosus10
Novel biallelic mutations in the DUOX2 gene underlying very early-onset inflammatory bowel disease: A case report10
CXCL5 inhibition improves kidney function by protecting renal tubular epithelial cells in diabetic kidney disease10
Effect of monoclonal antibody therapy on the endogenous SARS-CoV-2 antibody response10
A homozygous loss-of-function C1S mutation is associated with Kikuchi-Fujimoto disease10
Recurrent tandem duplication of UNC13D in familial hemophagocytic lymphohistiocytosis type 310
Immunological abnormalities in patients with early-onset ataxia with ocular motor apraxia and hypoalbuminemia10
Tissue resident cell processes determine organ damage in systemic lupus erythematosus10
From mice to men: An assessment of preclinical model systems for the study of vitiligo10
Genetic variant within CDK6 regulates immune response to palbociclib treatment10
Enhanced fatty acid oxidation by selective activation of PPARα alleviates autoimmunity through metabolic transformation in T-cells10
Tissue-resident memory T cells exhibit phenotypically and functionally heterogeneous in human physiological and pathological nasal mucosa10
Anti-IL12p40 autoantibodies in a teenage girl with multiple recurrent abscesses9
Comorbid association of obstructive sleep apnea (OSA) and thrombotic primary antiphospholipid syndrome (tPAPS): A more severe phenotype?9
Corrigendum to “Engineering bispecific T-cell engagers to deplete eosinophils for the treatment of severe eosinophilic asthma” [Clinical Immunology 255 (2023) 109755]9
IKAROS gain of function disease: Allogeneic hematopoietic cell transplantation experience and expanded clinical phenotypes9
Modulation of bone marrow and peripheral blood cytokine levels by age and clonal hematopoiesis in healthy individuals9
Common hematological values predict unfavorable outcomes in hospitalized COVID-19 patients9
Long non-coding RNA: Multiple effects on the differentiation, maturity and cell function of dendritic cells9
Behçet's disease with a somatic UBA1 variant:Expanding spectrum of autoinflammatory phenotypes of VEXAS syndrome9
Corrigendum to “cardiac pathology and outcomes vary between Kawasaki disease and PIMS-TS” clinical immunology 229 (2021) 1087809
Dark pigmentation and related low FMOD expression increase IL-3 and facilitateplasmacytoid dendritic cell maturation9
Alterations in exhausted and classical memory B cells in lupus nephritis – Relationship with disease relapse9
TACI and endogenous APRIL in B cell maturation9
The pathogenesis of obstetric APS: a 2023 update9
Th2 cell clonal expansion at diagnosis in human type 1 diabetes9
A spectrum of novel anti-vascular endothelial cells autoantibodies in idiopathic nephrotic syndrome patients9
Comprehensive analysis of ncRNA involvement in brain microglia immunology9
Pulmonary and systemic effects of inhaled crystalline silica in the HOCl-induced mouse model of systemic sclerosis: An experimental model of Erasmus syndrome.9
IL-10-producing regulatory cells impact on celiac disease evolution9
Benralizumab affects NK cell maturation and proliferation in severe asthmatic patients9
“Untargeting” autoantibodies using genome editing, a proof-of-concept study9
Integration of metabolomics and lipidomics reveals serum biomarkers for systemic lupus erythematosus with different organs involvement8
Comprehensive characterization of costimulatory molecule gene for diagnosis, prognosis and recognition of immune microenvironment features in sepsis8
Type I interferon activation in RAS-associated autoimmune leukoproliferative disease (RALD)8
USP18 induction regulates immunometabolism to attenuate M1 signal-polarized macrophages and enhance IL-4-polarized macrophages in systemic lupus erythematosus8
Intravenous immunoglobulin in kidney transplantation: Mechanisms of action, clinical applications, adverse effects, and hyperimmune globulin8
METTL3/16-mediated m6A modification of ZNNT1 promotes hepatocellular carcinoma progression by activating ZNNT1/osteopontin/S100A9 positive feedback loop-mediated crosstalk between macrophages and tumo8
Lactobacillus rhamnosus (LR) ameliorates pulmonary and extrapulmonary acute respiratory distress syndrome (ARDS) via targeting neutrophils8
Non-criteria antiphospholipid antibodies and calprotectin as potential biomarkers in pediatric antiphospholipid syndrome8
The role of neutrophils in autoimmune diseases8
Sialylated IVIg binding to DC-SIGN+ Hofbauer cells induces immune tolerance through the caveolin-1/NF-kB pathway and IL-10 secretion8
The Tmod cellular logic gate as a solution for tumor-selective immunotherapy8
Lupus gut microbiota transplants cause autoimmunity and inflammation8
The enome-wide ssociation tudy of erum IgE evels emonstrated a hared enetic ackground in llergic iseases8
Sequential administration of anti-complement component C5 eculizumab and type-2 anti-CD20 obinutuzumab for the treatment of early antibody-mediated rejection after kidney transplantation: A proof of c8
How to overcome tumor resistance to anti-PD-1/PD-L1 therapy by immunotherapy modifying the tumor microenvironment in MSS CRC8
Comprehensive characterization of pathogenic synovial fluid extracellular vesicles from knee osteoarthritis8
Long-term impact of congenital toxoplasmosis on phenotypic and functional features of circulating leukocytes from infants one year after treatment onset8
PReS-endorsed international childhood lupus T2T task force definition of childhood lupus low disease activity state (cLLDAS)8
Endoplasmic reticulum stress impairs the immune regulation property of macrophages in asthmatic patients8
Evaluating patient immunocompetence through antibody response to pneumococcal polysaccharide vaccine using a newly developed 23 serotype multiplexed assay8
CD169 expression on monocytes as a marker for assessing type I interferon status in pediatric inflammatory diseases8
Results of a Phase 3 Trial of an Oral CXCR4 Antagonist, Mavorixafor, for Treatment of Patients With WHIM Syndrome8
Classification of systemic lupus erythematosus in children and adults8
Identification of connective tissue disease autoantibodies and a novel autoantibody anti-annexin A11 in patients with “idiopathic” interstitial lung disease8
Characteristics of patients with low serum IgE levels and selective IgE deficiency: Data from an immunodeficiency referral center7
Profiling of mouse and human liver diseases identifies targets for therapeutic treatment of autoimmune hepatitis7
Cytomegalovirus infection is associated with thymic dysfunction and chronic graft-versus-host disease after pediatric hematopoietic stem cell transplantation7
Two novel compound heterozygous loss-of-function mutations cause fetal IRAK-4 deficiency presenting with Pseudomonas Aeruginosa sepsis7
Crosstalk between TRPV1 and immune regulation in Fuchs endothelial corneal dystrophy7
NETosis promotes chronic inflammation and fibrosis in systemic lupus erythematosus and COVID-197
LL37/self-DNA complexes mediate monocyte reprogramming7
Novel therapeutic strategies targeting abnormal T-cell signaling in systemic lupus erythematosus7
Gut vascular barrier in the pathogenesis and resolution of Crohn's disease: A novel link from origination to therapy7
Spesolimab rapidly treats generalized pustular psoriasis and improves the skin immune microenvironment in Chinese patients7
Single-cell profiling identifies T cell subsets associated with control of tuberculosis dissemination7
A novel application of delayed-type hipersensitivity reaction to measure cellular immune response in SARS-CoV-2 exposed individuals7
PARP14 promotes the growth and glycolysis of acute myeloid leukemia cells by regulating HIF-1α expression7
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