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 2021-05-01 to 2025-05-01.)
ArticleCitations
Primary immunodeficiency associated with a SAMD9L mutation167
Effectiveness of T2 biologics in patients with common variable immune deficiency and allergic respiratory disease146
Exploring the role of insulin-like growth factor binding protein-1 in identifying idiopathic multicentric Castleman's disease types: Implications for the mTOR signaling pathway94
Assessment of disease activity and management of patients with NFkB1 insufficiency90
IgG Replacement Therapy Use in Patients with Hypogammaglobulinemia after Lung Transplant74
Editorial Board61
The possible involvement of sema3A and sema4A in the pathogenesis of multiple sclerosis57
Results of a Phase 3 Trial of an Oral CXCR4 Antagonist, Mavorixafor, for Treatment of Patients With WHIM Syndrome56
NLRP12-associated autoinflammatory disease: A novel causal mutation and bioinformatics analyses51
Large deletion in 6q containing the TNFAIP3 gene associated with autoimmune lymphoproliferative syndrome48
Tissue resident cell processes determine organ damage in systemic lupus erythematosus47
Anti-IL12p40 autoantibodies in a teenage girl with multiple recurrent abscesses47
Determining reference ranges for lymphocyte proliferation responses to phytohemagglutinin and Bacillus Calmette–Guérin in Iranian children45
USP18 induction regulates immunometabolism to attenuate M1 signal-polarized macrophages and enhance IL-4-polarized macrophages in systemic lupus erythematosus43
PReS-endorsed international childhood lupus T2T task force definition of childhood lupus low disease activity state (cLLDAS)42
2 Maternal and neonate outcomes following exposure to hyaluronidase-facilitated subcutaneous immunoglobulin 10% during pregnancy: a retrospective case series based on US claims data41
17 Severe Cardiac Tamponade in an Unusual Case of CTLA-4 Haploinsufficiency40
117 Clinical and Immunologic Phenotype of Prolidase Deficiency38
94 Compound heterozygous mutations in the kinase domain of IKKα lead to immunodeficiency and immune dysregulation38
195 DHR-based Flow Cytometry Beyond CGD37
5-HT is associated with the dysfunction of regulating T cells in patients with allergic rhinitis36
87 Phenotypic variability of Circulating Natural Killer Cells in healthy donors36
71 Two allelic variants in the SERPING1 gene associated with hereditary angioedema detected in one adult patient without clinical manifestation of the disease. Case report36
Age-dependent transcriptomic profiles of leukocytes in pediatric population35
AXL+SIGLEC6+ dendritic cells in cerebrospinal fluid and brain tissues of patients with autoimmune inflammatory demyelinating disease of CNS34
Distinct innate and adaptive immunity phenotypic profile at the circulating single-cell level in Psoriatic Arthritis34
Dok-1 regulates mast cell degranulation negatively through inhibiting calcium-dependent F-actin disassembly32
Novel biallelic mutations in the DUOX2 gene underlying very early-onset inflammatory bowel disease: A case report32
A spectrum of novel anti-vascular endothelial cells autoantibodies in idiopathic nephrotic syndrome patients32
142 A non-consanguineous family with hepatic veno-occlusive disease and immunodeficiency32
Modulation of bone marrow and peripheral blood cytokine levels by age and clonal hematopoiesis in healthy individuals31
Ionic reverberation modulates the cellular fate of CD8+tissue resident memory T cells (TRMs) in patients with renal cell carcinoma: A novel mechanism31
AIM2 inflammasome: A potential therapeutic target in ischemic stroke30
Sialylated IVIg binding to DC-SIGN+ Hofbauer cells induces immune tolerance through the caveolin-1/NF-kB pathway and IL-10 secretion30
Characterization of PANoptosis patterns predicts survival and immunotherapy response in gastric cancer30
Presence of ectopic germinal center structures in autoimmune hepatitis30
Characteristics of patients with low serum IgE levels and selective IgE deficiency: Data from an immunodeficiency referral center29
Behçet's disease with a somatic UBA1 variant:Expanding spectrum of autoinflammatory phenotypes of VEXAS syndrome29
Lupus gut microbiota transplants cause autoimmunity and inflammation29
Editorial Board28
Pandemic chilblains: Are they SARS-CoV-2-related or not?27
Abnormal Newborn Screening for Severe Combined Immunodeficiency due to CD4 T cell lymphopenia associated with Heterozygous FOXN1 Variants in the Forkhead Domain27
Ectopic lymphoid structures in the aged lacrimal glands27
Immune dysregulation in children with inherited bone marrow failure syndromes and refractory cytopenia of childhood27
Clinical relevance of somatic mosaic variants detected from exome sequencing data27
Successful Management of Malakoplakia in a Patient Combined Variable Immunodeficiency26
127 Autoimmune Lymphoproliferative Syndrome or Autoimmune Lymphoproliferative Syndrome-Like? Why the Genetic Distinction Matters25
40 A case report description of a patient with CVID and Granulomatous Interstitial Nephritis25
Retrospective Study on Vaccine Responses and Natural Course of COVID-19 Infections in Primary Immunodeficiency25
165 The neuroimmunological network in cancer-induced HPV Infections25
39 An educational outreach to identify racial and ethnic disparity awareness in immunodeficiency patient care25
OX40 shapes an inflamed tumor immune microenvironment and predicts response to immunochemotherapy in diffuse large B-cell lymphoma25
124 Neutropenia in X-linked agammaglobulinemia patients, is possibly the most common presenting sign25
Changes in mucosal IgG4+- and IL-10+-cell frequencies in adults with eosinophilic esophagitis on a two-food elimination diet25
Interaction between Ras and Bcl2L12 in B cells suppresses IL-10 expression24
Elevated expression of receptors for EGF, PDGF, transferrin and folate within murine and human lupus nephritis kidneys23
Cutaneous T-cell lymphoma as a unique presenting malignancy in X-linked magnesium defect with EBV infection and neoplasia (XMEN) disease23
“Oral Manifestations of Patients with Inherited Defect in Phagocyte Number or Function” a systematic review23
Stem cell transplantation as treatment for major histocompatibility class I deficiency23
Chemotherapy for a secondary malignancy nearly restores complete chimerism in an SCID-patient after HSCT23
Corrigendum to “Convergent CDR3 homology amongst Spike-specific antibody responses in convalescent COVID-19 subjects receiving the BNT162b2 vaccine” [Clinical Immunology 237 (2022) 108963]23
Targeted metabolomics combined with machine learning to identify and validate new biomarkers for early SLE diagnosis and disease activity23
Biological effect of PM10 on airway epithelium-focus on obstructive lung diseases23
Novel therapeutic strategies targeting abnormal T-cell signaling in systemic lupus erythematosus23
Update of evidence- and consensus-based guidelines for the treatment of juvenile idiopathic arthritis (JIA) by the German Society of Pediatric and Juvenile Rheumatic Diseases (GKJR): New perspectives 22
Clinical and laboratory predictors of monogenic very early onset inflammatory bowel disease22
Interplay of redox imbalance with matrix gelatinases in neutrophils and their association with disease severity in rheumatoid arthritis patients22
WITHDRAWN: Border-associated macrophages in the central nervous system21
5 How do non-infectious presentations begin in patients with Inborn Errors of Immunity?20
Functional consequence of Iron dyshomeostasis and ferroptosis in systemic lupus erythematosus and lupus nephritis20
Transcriptomic studies unravel the molecular and cellular complexity of systemic lupus erythematosus: A review20
45 Assessment of TREC-based NBS SCID reporting practices for harmonization of results and interpretation: a global survey20
Histological evidence of MAPK pathway activation across subtypes of adult orbital xanthogranulomatous disease irrespective of the detection of oncogenic mutations20
123 Helper T cell immunity in humans with inherited CD4 deficiency20
Targeting autophagy regulation in NLRP3 inflammasome-mediated lung inflammation in COVID-1920
Epigenetic regulation is involved in traffic-related PM2.5 aggravating allergic airway inflammation in rats20
Seroconversion among rituximab-treated patients following SARS-CoV-2 vaccine supplemental dose19
Broadly neutralizing antibodies targeting HIV: Progress and challenges19
The role of podocytes in lupus nephritis: Insights and implications19
Comparing the immune abnormalities in MIS-C to healthy children and those with inflammatory disease reveals distinct inflammatory cytokine production and a monofunctional T cell response19
Better efficacy, lower recurrence rate and decreased CD8+TRM with guselkumab treatment for generalized pustular psoriasis: A prospective cohort study from China19
196 Unique Presentation of Mycobacterium haemophilum, Associated with T-cell dysfunction after Nelarabine Administration18
The CD14++CD16+ monocyte subset is expanded and controls Th1 cell development in Graves' disease18
Antiphospholipid syndrome nephropathy: Current knowledge and unanswered questions18
Pancreatic sympathetic innervation disturbance in type 1 diabetes18
Effect of repurposed metabolic drugs on human macrophage polarization and antitumoral activity18
The effect of early life cytomegalovirus infection on the immune profile of children18
HLA evolutionary divergence effect on bacterial infection risk in cirrhotic liver transplant candidates18
Combination therapy with immune checkpoint inhibitors in advanced renal cell carcinoma: A meta-analysis of randomized controlled trials18
PD-1 signaling pathway in sepsis: Does it have a future?18
Immune evasion and chronological decrease in titer of neutralizing antibody against SARS-CoV-2 and its variants of concerns in COVID-19 patients18
Monogenic inflammatory bowel disease with STXBP2 mutations is not resolved by hematopoietic stem cell transplantation but can be alleviated via immunosuppressive drug therapy18
Resolution of IgA vasculitis nephritis in patient with activated PI3Kdelta syndrome after treatment with leniolisib17
Monogenic inborn errors of immunity in autoimmune disorders17
Lymphocyte disturbance and functional assessment of the [Asp521Asn] ZAP70 mutation17
Extracellular vesicles derived from the intestinal microbiota of patients with CGD-associated inflammatory bowel disease have pro-inflammatory effects17
Report of TSPEAR Variants, the Hypereosinophilic Syndrome, and Severe Atopy17
Editorial Board17
Comparison of 3 anti-PLA2R inmmunoassaysfor the diagnosis of idiopathic membranous nephropathy in an european population. A pilot study17
Dominant interfering CARD11 variants disrupt JNK signaling in T cells and impaired CARD11-JNK signaling increases expression of GATA317
A New Registry for Genetic Diagnosis of Inborn Errors of Immunity within the Military Health System17
Interleukin-7 and soluble Interleukin-7 receptor levels in type 1 diabetes – Impact of IL7RA polymorphisms, HLA risk genotypes and clinical features17
Effects of dietary restriction on gut microbiota and CNS autoimmunity16
Real world treatment of juvenile-onset systemic lupus erythematosus: Data from the UK JSLE cohort study16
50 Utilizing an Ethical Lens to Assess a Series of Patients With X-Linked CGD Who Did Not Undergo Hematopoietic Stem Cell Transplant16
A heterozygous CARD11 variant in a patient with infantile atopic disease, humoral deficiency and lymphocytosis16
153 Demyelinating CNS Disease: An Unusual Complication of XLA16
The FCGR2A rs1801274 polymorphism was associated with the risk of death among COVID-19 patients16
From homeostasis to defense: Exploring the role of selective autophagy in innate immunity and viral infections16
203 Seronegative Autoimmune Hepatitis Complicated by Severe Aplastic Anemia16
Lymphoproliferation- a clue towards an underlying monogenic disorder of immune dysregulation- a retrospective analysis from a single center in India16
Interleukin 35 contributes to immunosuppression by regulating inflammatory cytokines and T cell populations in the acute phase of sepsis16
Serum proteome and metabolome uncover novel biomarkers for the assessment of disease activity and diagnosing of systemic lupus erythematosus16
190 What is needed to diagnose an autoinflammatory disease? From clinical manifestations to genomic sequencing: the Brazilian experience16
104 PD-1 Inhibition with Nivolumab Can Cure EBV-driven Lymphoproliferative Disorders, Avoiding Need for Toxic Allogeneic Bone Marrow Transplantation16
Monoclonal gammopathy in autoimmune diseases: Analysis and follow-up of 160 cases in a tertiary center in China16
ACase of GATA2 Deficiency with Pancytopenia and Recurrent Infections: To Transplant or Not to Transplant?15
Recent advances in the involvement of epigenetics in the pathogenesis of systemic lupus erythematosus15
Pediatric lymphoproliferative disorders associated with inborn errors of immunity15
Detection of immunoglobulin response to COVID-19 vaccination using a novel rapid fingerstick assay15
A Case of Pneumocystis jirovecii Pneumonia in an Infant with Ataxia-Pancytopenia Syndrome15
HSV-1 and HHV-6 Meningoencephalitis in a Child with STAT1 Mutation15
Consensus gene modules strategy identifies candidate blood-based biomarkers for primary Sjögren's disease15
Resolving Incomplete Penetrance in Primary Immunodeficiencies15
Beyond the classics: The emerging value of anti-phosphatidylserine/prothrombin antibodies in antiphospholipid syndrome15
Selective production of IL-33-neutralizing autoantibody ameliorates asthma responses and severity15
Reconstruction of Sjögren's syndrome-like sialadenitis by a defined disease specific gut-reactive single TCR and an autoantibody15
Should we be targeting type 1 interferons in antiphospholipid syndrome?14
Integrated analysis of ATAC-seq and RNA-seq reveals the chromatin accessibility and transcriptional landscape of immunoglobulin a nephropathy14
Renal dysfunction in AQP4 NMOSD and MS; a potential predictor of relapse and prognosis14
Clinical, immunological, molecular and therapeutic findings in monogenic immune dysregulation diseases: Middle East and North Africa registry14
A nomogram for the prediction of co-infection in MDA5 dermatomyositis: A rapid clinical assessment model14
Local injection of micro-dose anti-interleukin-17A antibody for palmoplantar pustulosis: A real-world study14
Age-specific Metabolomic profiles in children with food allergy14
Liraglutide protects β-cells in novel human islet spheroid models of type 1 diabetes14
Health-related quality of life in primary immunodeficiencies: Impact of delayed diagnosis and treatment burden14
Clinical trait-specific genetic analysis in Behçet's disease identifies novel loci associated with ocular and neurological involvement14
Editorial Board14
Single-cell mapping reveals dysregulation of immune cell populations and VISTA+ monocytes in myasthenia gravis14
From discovery to approval: A brief history of the compstatin family of complement C3 inhibitors14
Stem cell like memory T cells: A new paradigm in cancer immunotherapy13
Menthol nanoliposomes enhanced anti-tumor immunotherapy by increasing lymph node homing of dendritic cell vaccines13
Hypoxia-induced ALKBH5 aggravates synovial aggression and inflammation in rheumatoid arthritis by regulating the m6A modification of CH25H13
Anti-phospholipid autoantibodies in human diseases13
Characterization of primary Sjögren's syndrome in the Taiwan Han population through a genome-wide association study and polygenic risk score analysis13
PPARγ inhibits small airway remodeling through mediating the polarization homeostasis of alveolar macrophages in COPD13
Telomere biology disorders may manifest as common variable immunodeficiency (CVID)13
Memory CD4+T cell profile is associated with unfavorable prognosis in IgG4-related disease: Risk stratification by machine-learning13
MAIT cells confer resistance to Lenvatinib plus anti-PD1 antibodies in hepatocellular carcinoma through TNF-TNFRSF1B pathway13
Itaconate reduces proliferation and migration of fibroblast-like synoviocytes and ameliorates arthritis models13
Novel heterozygous SPI1c.538C>T p.(Leu180Phe) variant causes PU.1 haploinsufficiency leading to agammaglobulinemia13
Anti-inflammatory and immune therapy in severe coronavirus disease 2019 (COVID-19) patients: An update13
Abatacept for treatment-refractory pediatric CTLA4-haploinsufficiency13
Proteomic profiling of aqueous humor-derived exosomes in Vogt-Koyanagi-Harada disease and Behcet's uveitis13
96 Molecular and functional identification of unstable regulatory and autoreactive effector T cells that are expanded in patients with FOXP3 mutation12
99 C-terminal mutants in IRF8 associated with mild natural killer cell deficiency12
Longitudinal observation of antibody responses for 14 months after SARS-CoV-2 infection12
Patient Perspectives on Adaptation to Inborn Errors of Immunity12
Treatment of multiple sclerosis in children: A brief overview12
139 Novel CARD14 Variant: ACase of Autoinflammatory Disorder in a 5-Year-Old with Therapeutic Insights12
98 Unique challenges and unique solutions in hematopoietic stem cell transplantation for rare inborn errors of immunity12
Natural supplements in antiphospholipid syndrome: A case for further study12
Another iceberg of genetic testing: more questions than answers12
85 Navigating the Gray Area: Borderline Hemophagocytic Lymphohistiocytosis Criteria and Dilemmas in Diagnosis and Treatment – A Case Report12
A distinct association of inflammatory molecules with outcomes of COVID-19 in younger versus older adults12
Domain 5 of Beta 2 glycoprotein I: Friend or foe in health? Context matters12
Progressive multifocal leukoencephalopathy (PML) treated with pembrolizumab in a patient with mosaic STAT3 gain-of-function mutation12
Defining the impact of FOXN1 variants with functional assays and reaggregate thymus organ cultures reveals those with loss- and gain- of function and dominant negative consequences11
Assessment of commonly used methods to determine myelin-reactivity of T cells in multiple sclerosis11
CaMK4 expression on effector memory T cells is associated with organ damage in systemic lupus erythematosus: A case report11
A distinct immunophenotype in children carrying the Blautia enterotype: The Generation R study11
Limitations in the clinical utility of vaccine challenge responses in the evaluation of primary antibody deficiency including Common Variable Immunodeficiency Disorders11
Sex-based comparison of CD4+ T cell DNA methylation in lupus reveals proinflammatory epigenetic changes in men11
Interstitial cystitis in common variable immunodeficiency: Could it be another autoimmune complication? A descriptive report11
Delayed onset ADA-SCID presenting as secondary HLH in a patient with normal newborn screening11
Increased expression of Clec9A on cDC1s associated with cytotoxic CD8+ T cell response in COPD11
Ruxolitinib attenuates acute rejection and can serve as an immune induction therapy in heart transplantation11
Rare Turner syndrome and lupus coexistence with insights from DNA methylation patterns11
Microsporum gypseum infection among two related families, with a zoonotic aspect: a prospective case series11
Editorial Board11
Attenuation of renal injury by depleting cDC1 and by repurposing Flt3 inhibitor in anti-GBM disease11
LXA4 protected mice from renal ischemia/reperfusion injury by promoting IRG1/Nrf2 and IRAK-M-TRAF6 signal pathways11
Regulatory T cell homeostasis: Requisite signals and implications for clinical development of biologics11
Negative impact of Interleukin-9 on synovial regulatory T cells in rheumatoid arthritis10
Insights into the multifaceted role of interleukin-37 on human immune cell regulation10
Leveraging pleiotropy identifies common-variant associations with selective IgA deficiency10
Kappa-index: Real-life evaluation of a new tool for multiple sclerosis diagnosis10
147 DiGeorge Syndrome with an atypical presentation: Lymphoproliferation and malignancy10
74 Getting to the Heart of the Cause: Epidermodysplasia verruciformis in a Patient Born with Transposition of the Great Arteries and Mosaic Turner Syndrome10
Detection of anti-mitochondrial 2-oxoacid dehydrogenase complex subunit's antibodies for the diagnosis of Primary Biliary Cholangitis10
Allergy and autoinflammation drive persistent systemic inflammatory response in Meniere Disease: A longitudinal study10
ROCK2, a critical regulator of immune modulation and fibrosis has emerged as a therapeutic target in chronic graft-versus-host disease10
158 Good Syndrome: A Case of Bowel Perforation, Chronic Diarrhea and Clostridium Difficile Colitis Leading to Detection of a Thymoma10
42 Severe Combined Immunodeficiency Due To A Monoallelic ITPR3 Variant Presenting With Lymphohistiocytosis And Bone Marrow Failure Treated With Myeloablative Hematopoietic Cell Transplantation10
92 Selective IgA Deficiency in a Patient with Susac Syndrome10
The immune cell transcriptome is modulated by vitamin D3 supplementation in people with a first demyelinating event participating in a randomized placebo-controlled trial10
Characterization of immune responses associated with ERAP-1 expression in HSV-induced Behçet's disease mouse model10
NLRC4 gain-of-function variant is identified in a patient with systemic lupus erythematosus10
New laboratory criteria of the autoimmune inflammation in pulmonary sarcoidosis and tuberculosis10
47 Pharmacokinetics, efficacy, and safety of weekly/biweekly dosing of Xembify® in treatment-experienced patients, and loading/maintenance dosing in treatment-naïve patients with primary immunodeficie10
55 Diagnostic utility of the whole blood transcriptome and mucosal microbiome alterations in patients with primary immunodeficiency10
Challenges for gene editing in common variable immunodeficiency disorders: Current and future prospects10
A large deletion in a non-coding regulatory region leads to NFKB1 haploinsufficiency in two adult siblings9
Behçet disease, familial Mediterranean fever and MEFV variations: More than just an association9
Augmented oxidative stress, accumulation of DNA damage and impaired DNA repair mechanisms in thrombotic primary antiphospholipid syndrome9
Human glycoprotein-2 expressed in Brunner glands – A putative autoimmune target and link between Crohn's and coeliac disease9
De novo molecular subtyping of salivary gland tissue in the context of Sjögren's syndrome heterogeneity9
Insights Through Detailed Immunophenotyping into The Immune Etiology Of Indeterminate Pediatric Acute Liver Failure (IND-PALF): An Immune Dysregulatory Disease9
Quality of Life in Patients with Predominant Antibody Deficiency9
Cancer germline antigen gene MAGEB2 promotes cell invasion and correlates with immune microenvironment and immunotherapeutic efficiency in laryngeal cancer9
Protective immunity to repeated COVID-19 breakthrough infections9
Metabolic landscape dysregulation in bronchoalveolar lavage fluid of checkpoint inhibitor pneumonitis9
ICOS agonist vopratelimab modulates follicular helper T cells and improves B cell function in common variable immunodeficiency9
Deep sequencing refines prior genomic analysis in families with apparent gonadal mosaicism9
159 A Case of Eosinophilic Fasciitis Successfully Managed with Benralizumab in a Patient with Hypogammaglobulinemia and B-cell Aplasia9
Clinical and immunological prophyle of long lasting and late onset neutropenia: beyond primary autoimmune and idiopathic neutropenia9
ALPS Diagnosis: Different Phenotype in Child and Mother9
Characterization of AR-CGD female patient with a novel homozygous deletion in CYBC1 gene presenting with unusual clinical phenotype9
Broad applicability of the Goldspire™ platform for the treatment of solid tumors9
Hyper IgE syndromes: A clinical approach9
What can we learn from DNA methylation studies in lupus?9
Editorial Board9
TREC/KREC indicators in newborns at gestation 28–34 weeks9
Maternal Health Characteristics Associated with Idiopathic T Cell Lymphopenia of Infancy8
A tetravalent bispecific antibody outperforms the combination of its parental antibodies and neutralizes diverse SARS-CoV-2 variants8
B-cell driven autoimmunity in two patients with monogenic autoinflammatory disorders8
Type I interferon activation in RAS-associated autoimmune leukoproliferative disease (RALD)8
57 Development and Implementation of the TRIO Health Activated Phosphoinositide 3-kinase Delta Syndrome Characterization and Clinical Outcomes Immunologic Registry (APDS-CHOIR)8
108 PU.1-associated inborn errors of immunity: new mutations, phenotypes, and inheritance patterns8
The enome-wide ssociation tudy of erum IgE evels emonstrated a hared enetic ackground in llergic iseases8
“Untargeting” autoantibodies using genome editing, a proof-of-concept study8
Impact of Early Intervention for STAT3 Dominant-Negative Disease8
Dupilumab as Adjunct Treatment for Persistent Food Allergy in Adulthood8
Neutrophil extracellular traps promote macrophage inflammation in psoriasis8
The Use of Novel Antibodies to Characterize B cells in Health and Disease8
Could Osteopontin be a useful biomarker in the diagnosis and severity assessment of osteoarthritis? A systematic review and meta-analysis of recent evidence8
19 POLD3 deficiency is associated with syndromic severe combined immunodeficiency including neurodevelopmental delay and hearing impairment8
29 Safety and feasibility of the use of dual cardiac-thymus transplant in a child with cardiac failure requiring heart transplant8
Exhaustion and over-activation of immune cells in COVID-19: Challenges and therapeutic opportunities8
Family History of Agammaglobulinemia Among Racial and Ethnic Minority Groups with X-linked Agammaglobulinemia from the USIDNET Registry8
A Case of X-Linked Moesin-Associated Immune Deficiency in a Pediatric Patient8
CD32 (FcγRIIB) expression is low on CD21low B cells from systemic sclerosis patients with digital ulcers, interstitial lung disease, and anti-topoisomerase I autoantibodies8
Ex vivo T-lymphopoiesis assays assisting corrective treatment choice for genetically undefined T-lymphocytopenia8
Toll-like receptor 10 expression in B cells is negatively correlated with the progression of primary Sjögren's disease8
Cyclic helix B peptide ameliorated the sepsis-induced injury in human HPMEC cells through regulating NF-κB8
176 JAK1-selective inhibitor upadacitinib induced dynamic immunologic alterations and clinical response in treatment-resistant CVID gastrointestinal disease8
166 PRF1-Related Isolated CNS Hemophagocytic Lymphohistiocytosis Successfully Treated with Ruxolitinib Monotherapy8
Association of KIR gene polymorphisms with COVID-19 disease8
RAC2 mutations and immune deficiency – functional spectrum of an international cohort8
8 Impact of plasma collection date on antibodies to SARS-CoV-2 in intravenous immunoglobulin7
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