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CD4+T cells and natural killer cells: Biomarkers for hepatic fibrosis in human immunodeficiency virus/hepatitis C viruscoinfected patients
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CD4+T cells and natural killer cells: Biomarkers for hepatic fibrosis in human immunodeficiency virus/hepatitis C viruscoinfected patients
Laufer, Natalia Lorna et al · Baishideng Publishing Group Co · 2017 · ISSN 1073-1080
To characterize peripheral blood natural killer (NK) cells phenotypes by flow cytometry as potential biomarker of liver fibrosis in human immunodeficiency virus (HIV)/hepatitis C virus (HCV) coinfected patients. Samples ...
Idioma eng
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Investigating serum free light chains in patients with common variable immunodeficiency disorder in compare with other immunodeficiency diseases
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Investigating serum free light chains in patients with common variable immunodeficiency disorder in compare with other immunodeficiency diseases
Mohammad Hassan Bemanian et al · Nature Portfolio · 2026 · ISSN 2045-2322
Abstract Serum free light chains (sFLCs) have recently been introduced as a diagnostic biomarker in common variable immunodeficiency (CVID) patients. Most patients with CVID have undetectable or lower levels of sFLCs com...
LCC LCC:Medicine; TENDOlNjaWVuY2U~Idioma eng
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Ocorrência do vírus da imunodeficiência felina e do vírus da leucemia felina em gatos domésticos mantidos em abrigos no município de Belo Horizonte Occurrence of feline immunodeficiency virus and feline leukemia virus in Sheltered domestic cats of Belo Horizonte
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Ocorrência do vírus da imunodeficiência felina e do vírus da leucemia felina em gatos domésticos mantidos em abrigos no município de Belo Horizonte Occurrence of feline immunodeficiency virus and feline leukemia virus in Sheltered domestic cats of Belo Horizonte
B.M. Teixeira et al · Universidade Federal de Minas Gerais, Escola de Veterinária · 2007 · ISSN 0102-0935
Investigou-se a ocorrência da infecção pelo vírus da imunodeficiência felina (FIV) e pelo vírus da leucemia felina (FeLV) em gatos domésticos, provenientes de dois abrigos, no município de Belo Horizonte. Amostra...
LCC LCC:Animal cultureIdioma eng
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A Biallelic HELIOS Nonsense Mutation Disrupting Dimerization Is Associated with a Novel Syndromic Immunodeficiency
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A Biallelic HELIOS Nonsense Mutation Disrupting Dimerization Is Associated with a Novel Syndromic Immunodeficiency
Hye Sun Kuehn et al · Rockefeller University Press · 2026 · ISSN 3065-8993
HELIOS is an IKAROS-family zinc-finger transcription factor that plays an important role in regulatory T cell function and conventional T cell homoeostasis. HELIOS shares a conserved N-terminal DNA-binding and C-terminal...
LCC LCC:Immunologic diseases. AllergyIdioma eng
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A Site-Specific LLM-Based PHI Redaction Tool to Support Note De-Identification for the United States Immunodeficiency Network (USIDNET)
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A Site-Specific LLM-Based PHI Redaction Tool to Support Note De-Identification for the United States Immunodeficiency Network (USIDNET)
Vaibhavi Vichare et al · Rockefeller University Press · 2026 · ISSN 3065-8993
The United States Immunodeficiency Network (USIDNET) is a registry that collects de-identified patient data from hospitals across the country to study rare immune conditions, including inborn errors of immunity (IEI). Th...
LCC LCC:Immunologic diseases. AllergyIdioma eng
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A Whole-Blood Transcriptomic Assay, PrimDx, Reflects Cellular and Humoral Abnormalities in Primary Immunodeficiency
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A Whole-Blood Transcriptomic Assay, PrimDx, Reflects Cellular and Humoral Abnormalities in Primary Immunodeficiency
Holly Pedersen et al · Rockefeller University Press · 2026 · ISSN 3065-8993
Early diagnosis of primary immunodeficiency (PID) remains a significant clinical challenge, often delaying treatment and increasing the risk of severe infections. Accurate identification of antibody (Ab) deficiencies typ...
LCC LCC:Immunologic diseases. AllergyIdioma eng
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CXCL13 as a Biomarker of Complex Common Variable Immunodeficiency
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CXCL13 as a Biomarker of Complex Common Variable Immunodeficiency
Ioasaf Karafotias et al · Rockefeller University Press · 2026 · ISSN 3065-8993
Common variable immunodeficiency (CVID) is a group of heterogeneous disorders with common denominators of impaired antibody production and function and recurrent infections. Currently, prognostic biomarkers for CVID are ...
LCC LCC:Immunologic diseases. AllergyIdioma eng
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Characterizing Autoimmune and End-Organ Lympho-Infiltrative Disease Burden in Childhood-Onset Common Variable Immunodeficiency
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Characterizing Autoimmune and End-Organ Lympho-Infiltrative Disease Burden in Childhood-Onset Common Variable Immunodeficiency
Leon Reteig et al · Rockefeller University Press · 2026 · ISSN 3065-8993
BackgroundCommon variable immunodeficiency (CVID) is the most prevalent inborn error of immunity. Although CVID is most commonly diagnosed in adulthood, a subset of patients is diagnosed in childhood. Autoimmune and end-...
LCC LCC:Immunologic diseases. AllergyIdioma eng
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Clinical Implications of Baseline-Corrected Total Immunoglobulin G Levels: Pharmacokinetic Data from a Phase 3, Open-Label Study of Patients with Primary Immunodeficiency Disease Treated with fSCIG 10%
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Clinical Implications of Baseline-Corrected Total Immunoglobulin G Levels: Pharmacokinetic Data from a Phase 3, Open-Label Study of Patients with Primary Immunodeficiency Disease Treated with fSCIG 10%
Komal Prem et al · Rockefeller University Press · 2026 · ISSN 3065-8993
Dosing immunoglobulin G (IgG) replacement therapy in primary immunodeficiency disease (PIDD) depends on IgG pharmacokinetics (PK) and patients’ clinical status. Conventionally, PK data used to determine dosing were bas...
LCC LCC:Immunologic diseases. AllergyIdioma eng
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Combined Immunodeficiency Manifests from S-Adenosylhomocysteine (SAH) Hydrolase Deficiency
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Combined Immunodeficiency Manifests from S-Adenosylhomocysteine (SAH) Hydrolase Deficiency
Ian Cohn et al · Rockefeller University Press · 2026 · ISSN 3065-8993
S-adenosylhomocysteine (SAH) hydrolase deficiency is a rare autosomal recessive disorder caused by pathogenic variants of the gene AHCY. Loss of SAH hydrolase causes SAH accumulation and impairs the methionine/S-adenosyl...
LCC LCC:Immunologic diseases. AllergyIdioma eng
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Deletion of IRF2BP2 Presenting as Late-Onset Common Variable Immunodeficiency with Bronchiectasis
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Deletion of IRF2BP2 Presenting as Late-Onset Common Variable Immunodeficiency with Bronchiectasis
Samantha Shafer et al · Rockefeller University Press · 2026 · ISSN 3065-8993
Interferon regulatory factor-2-binding protein-2 (IRF2BP2) is a transcriptional regulator affecting diverse cellular functions, including cell differentiation and apoptosis. It plays an important role in lymphocyte and m...
LCC LCC:Immunologic diseases. AllergyIdioma eng
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Functional Defects in the NFκB pathway in Common Variable Immunodeficiency
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Functional Defects in the NFκB pathway in Common Variable Immunodeficiency
Terrence T.J. Hunter et al · Rockefeller University Press · 2026 · ISSN 3065-8993
Common variable Immunodeficiency (CVID) is a heterogeneous immunodeficiency characterized by hypogammaglobulinemia and immune dysregulation. In up to 30% of cases, there is a monogenic defect, with a fraction of these fa...
LCC LCC:Immunologic diseases. AllergyIdioma eng
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Genetics of B Cell Maturation in Common Variable Immunodeficiency in Brazil: A Joint Analysis of the CVID-Brazil Cohort and the CNE3I Program
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Genetics of B Cell Maturation in Common Variable Immunodeficiency in Brazil: A Joint Analysis of the CVID-Brazil Cohort and the CNE3I Program
Beatriz Costa Todt et al · Rockefeller University Press · 2026 · ISSN 3065-8993
Common variable immunodeficiency (CVID) is the most prevalent symptomatic primary immunodeficiency and remains underdiagnosed in Brazil due to limited knowledge of its genetic landscape. Since 2024, the Centro Nacional d...
LCC LCC:Immunologic diseases. AllergyIdioma eng
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Health-Related Quality of Life Reveals Distinct Fatigue and Functional Burden in Inflammatory Common Variable Immunodeficiency
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Health-Related Quality of Life Reveals Distinct Fatigue and Functional Burden in Inflammatory Common Variable Immunodeficiency
Andrew Wong-Pack et al · Rockefeller University Press · 2026 · ISSN 3065-8993
RationaleCommon variable immunodeficiency (CVID) is a chronic, multisystem immune disorder associated with substantial symptom burden beyond infections, particularly among individuals with noninfectious inflammatory comp...
LCC LCC:Immunologic diseases. AllergyIdioma eng
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Heterogeneous CD21low B Cell Subsets and Their Functional Impact in Common Variable Immunodeficiency
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Heterogeneous CD21low B Cell Subsets and Their Functional Impact in Common Variable Immunodeficiency
Jitka Smetanová et al · Rockefeller University Press · 2026 · ISSN 3065-8993
Atypical CD21low B lymphocytes are a naturally occurring transient subset that has been increasingly recognized in chronic diseases, such as infections and immune dysregulation, where they may persist for long. Their fat...
LCC LCC:Immunologic diseases. AllergyIdioma eng
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INTERPRETATIVE PHENOMENOLOGICAL ANALYSIS MENGENAI PENGALAMAN MANTAN WARGA BINAAN DENGAN HUMAN IMMUNODEFICIENCY VIRUS
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INTERPRETATIVE PHENOMENOLOGICAL ANALYSIS MENGENAI PENGALAMAN MANTAN WARGA BINAAN DENGAN HUMAN IMMUNODEFICIENCY VIRUS
Fienna Anggita Siwi et al · Fakultas Psikologi Universitas Diponegoro · 2022 · ISSN 2337-375X
Seorang mantan Warga Binaan (WB) yang telah keluar dari Lembaga Permasyarakatan (Lapas) perlu melakukan penyesuaian dirinya untuk bisa kembali berbaur di tengah masyarakat. Begitupula secara spesifik mantan WB dengan Hum...
LCC TENDOlNwZWNpYWwgYXNwZWN0cyBvZiBlZHVjYXRpb24~Idioma eng
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IRF4 p.T95R Combined Immunodeficiency: Clinical Features and Transplant Outcomes
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IRF4 p.T95R Combined Immunodeficiency: Clinical Features and Transplant Outcomes
Mattison P. Stojcic et al · Rockefeller University Press · 2026 · ISSN 3065-8993
IntroductionInborn errors of interferon response factors (IRFs) are a subset of monogenic inborn errors of immunity, occurring as a result of damaging variants in the IRF genes. Of these diseases, IRF4 deficiencies are a...
LCC LCC:Immunologic diseases. AllergyIdioma eng
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Idiopathic Combined Immunodeficiency Associated with Primary Pulmonary Sporotrichosis
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Idiopathic Combined Immunodeficiency Associated with Primary Pulmonary Sporotrichosis
Marija Rowane et al · Rockefeller University Press · 2026 · ISSN 3065-8993
IntroductionSporotrichosis is an uncommon but emerging opportunistic infection in immunocompromised patients. Primary pulmonary sporotrichosis can disseminate and result in significant morbidity and mortality, despite tr...
LCC LCC:Immunologic diseases. AllergyIdioma eng
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Immune Thrombocytopenic Purpura as a Herald of Underlying X-Linked Immunodeficiency with Magnesium Defect, Epstein-Barr Virus Infection, and Neoplasia (XMEN) Disease in a Pediatric Patient
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Immune Thrombocytopenic Purpura as a Herald of Underlying X-Linked Immunodeficiency with Magnesium Defect, Epstein-Barr Virus Infection, and Neoplasia (XMEN) Disease in a Pediatric Patient
Kevin Lewis et al · Rockefeller University Press · 2026 · ISSN 3065-8993
BackgroundLoss-of-function variants in magnesium transporter 1 (MAGT1) cause X-linked Immunodeficiency with Magnesium defect, Epstein-Barr virus infection, and Neoplasia (XMEN) disease through impaired glycosylation. The...
LCC LCC:Immunologic diseases. AllergyIdioma eng
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NFKB1 Truncating Variants Associated with Significant Autoimmunity and Lymphoproliferation in Common Variable Immunodeficiency
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NFKB1 Truncating Variants Associated with Significant Autoimmunity and Lymphoproliferation in Common Variable Immunodeficiency
Chi Ma et al · Rockefeller University Press · 2026 · ISSN 3065-8993
Heterozygous NFKB1 variants have been increasingly identified in patients with common variable immunodeficiency. These patients, however, often experience substantial immune dysregulation beyond humoral deficiency. NFKB1...
LCC LCC:Immunologic diseases. AllergyIdioma eng
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Novel Pathogenic Variant in IL2RG Affecting the Signal Peptide Results in mRNA Instability, Decreased IL2RG Expression, and Atypical Late-Onset Immunodeficiency
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Novel Pathogenic Variant in IL2RG Affecting the Signal Peptide Results in mRNA Instability, Decreased IL2RG Expression, and Atypical Late-Onset Immunodeficiency
Muslima Hussain et al · Rockefeller University Press · 2026 · ISSN 3065-8993
X-linked severe combined immunodeficiency (SCID-X1) presents as T-B+NK- SCID, due to mutations in the common γ chain (IL2RG/CD132), a shared component of several cytokine receptors. Without definitive therapy, SCID-X1 i...
LCC LCC:Immunologic diseases. AllergyIdioma eng
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On-Demand Personalized Gene Editing to Treat IRF4 p.T95A Immunodeficiency
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On-Demand Personalized Gene Editing to Treat IRF4 p.T95A Immunodeficiency
Vasil Toskov et al · Rockefeller University Press · 2026 · ISSN 3065-8993
BackgroundOn-demand gene editing of autologous cells offers a novel therapeutic option for inborn errors of immunity (IEIs) caused by dominant-negative variants, which are often poorly addressed by conventional viral gen...
LCC LCC:Immunologic diseases. AllergyIdioma eng
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Overlap in Immunologic Pathways Between Asthma and Primary Immunodeficiency Disorders
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Overlap in Immunologic Pathways Between Asthma and Primary Immunodeficiency Disorders
Jooyoung Moon · Rockefeller University Press · 2026 · ISSN 3065-8993
BackgroundAsthma is traditionally conceptualized as a T helper 2 (Th2)-mediated inflammatory airway disease. However, increasing evidence suggests that primary immune dysregulation may underlie or phenotypically mimic as...
LCC LCC:Immunologic diseases. AllergyIdioma eng
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Quality of Life in Patients with Severe Combined Immunodeficiency (SCID) Treated with Hematopoietic Cell Transplantation in the Modern Era: A Primary Immune Deficiency Consortium (PIDTC) Study
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Quality of Life in Patients with Severe Combined Immunodeficiency (SCID) Treated with Hematopoietic Cell Transplantation in the Modern Era: A Primary Immune Deficiency Consortium (PIDTC) Study
Lauren Sanchez et al · Rockefeller University Press · 2026 · ISSN 3065-8993
IntroductionNewborn screening (NBS) for severe combined immunodeficiency (SCID) leads to early diagnosis and hematopoietic cell transplant (HCT). Limited studies are available on the quality of life (QoL) of SCID patient...
LCC LCC:Immunologic diseases. AllergyIdioma eng
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