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JOURNAL OF CLINICAL IMMUNOLOGY
ISSN：0271-9142

JOURNAL OF CLINICAL IMMUNOLOGY

J CLIN IMMUNOL
学科领域：医学
是否预警：不在预警名单内
是否OA：否
录用周期：平均2月
新锐分区：医学2区
年发文量：128
影响因子：5.7
JCR分区：Q1

基本信息

《临床免疫学杂志》发表人类免疫学领域的高影响力论文，探讨人类疾病的诊断、发病机制、预后或治疗。该杂志特别关注原发性免疫缺陷和相关疾病。这些包括先天性免疫缺陷，在广义上，它们的潜在基因型和它们的多样性表型，包括感染、恶性肿瘤、变态反应、自身炎症和自身免疫。我们考虑了这一领域的广泛研究，包括遗传发现、临床描述、免疫学评估、诊断方法、预后评估和治疗干预。如果病例报告是真正原创的，并附有相关医学文献的简明综述以及新病例研究如何推进该领域，则应予以考虑。四类论文详见作者须知。
0271-9142SCIE/Scopus收录
5.7
点击查看最新影响趋势>
4.2
新
2026年3月发布
点击查看历史分区趋势    >
大类学科小类学科Top期刊综述期刊
医学2区
IMMUNOLOGY 免疫学
2区
否
N/A
新
WOS期刊SCI分区  2024-2025最新升级版
按JIF指标学科分区收集子录JIF分区JIF排名百分位
学科：IMMUNOLOGY
SCIE
Q1
36/183
按JCR指标学科分区收集子录JCR分区JCR排名百分位
学科：IMMUNOLOGY
SCIE
Q1
34/183
87
128
点击查看年发文量趋势图>
2%0平均2月-医学-免疫学
10.5%
点击查看自引率趋势图>
时间预警情况
2026年03月发布的新锐学术版不在预警名单中
2025年03月发布的2025版不在预警名单中
2024年02月发布的2024版不在预警名单中
2023年01月发布的2023版不在预警名单中
2021年12月发布的2021版不在预警名单中
2020年12月发布的2020版不在预警名单中
90.63%50.26%8.65%
CiteScore：11.20
SJR：1.928
SNIP：1.588
学科类别分区排名百分位
大类：Medicine
小类：Immunology and Allergy
Q1
30 / 231
大类：Medicine
小类：Immunology
Q1
35 / 240

期刊高被引文献

Regulatory T Cells: the Many Faces of Foxp3
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Efficacy and Adverse Events During Janus Kinase Inhibitor Treatment of SAVI Syndrome
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Diagnostic Yield of Next Generation Sequencing in Genetically Undiagnosed Patients with Primary Immunodeficiencies: a Systematic Review
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WHIM Syndrome: from Pathogenesis Towards Personalized Medicine and Cure
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Haploidentical Stem Cell Transplantation with Post-Transplant Cyclophosphamide for Primary Immune Deficiency Disorders in Children: Challenges and Outcome from a Tertiary Care Center in South India
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Auto-inflammation in a Patient with a Novel Homozygous OTULIN Mutation
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Immune Dysregulation and Disease Pathogenesis due to Activating Mutations in PIK3CD—the Goldilocks’ Effect
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A Novel CARMIL2 Mutation Resulting in Combined Immunodeficiency Manifesting with Dermatitis, Fungal, and Viral Skin Infections As Well as Selective Antibody Deficiency
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Chronic Granulomatous Disease-Associated IBD Resolves and Does Not Adversely Impact Survival Following Allogeneic HCT
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Ficolin-3 Deficiency Is Associated with Disease and an Increased Risk of Systemic Lupus Erythematosus
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Fifteen Years of the J Project
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Health-Related Quality of Life and Emotional Difficulties in Chronic Granulomatous Disease: Data on Adult and Pediatric Patients from Italian Network for Primary Immunodeficiency (IPINet)
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Interstitial Lung Disease Frequently Precedes CVID Diagnosis
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A New Patient with Inherited TYK2 Deficiency
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Defining Primary Selective IgM Deficiency
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Altered Peripheral Blood Leucocyte Phenotype and Responses in Healthy Individuals with Homozygous Deletion of FHR1 and FHR3 Genes
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MiR-608 Exerts Anti-inflammatory Effects by Targeting ELANE in Monocytes
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Mutual alteration of NOD2-associated Blau syndrome and IFNγR1 deficiency
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NAPDH Oxidase-Specific Flow Cytometry Allows for Rapid Genetic Triage and Classification of Novel Variants in Chronic Granulomatous Disease
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Novel Exonic Deletions in TTC7A in a Newborn with Multiple Intestinal Atresia and Combined Immunodeficiency
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A De Novo Frameshift Mutation in TNFAIP3 Impairs A20 Deubiquitination Function to Cause Neuropsychiatric Systemic Lupus Erythematosus
来源期刊：Journal of Clinical ImmunologyDOI：10.1007/s10875-019-00695-4
Expanding Clinical Phenotype and Novel Insights into the Pathogenesis of ICOS Deficiency
来源期刊：Journal of Clinical ImmunologyDOI：10.1007/s10875-019-00735-z
Should MASP-2 Deficiency Be Considered a Primary Immunodeficiency? Relevance of the Lectin Pathway
来源期刊：Journal of Clinical ImmunologyDOI：10.1007/s10875-019-00714-4
Recurrent Salmonella typhi Infection and Autoimmunity in a Young Boy with Complete IL-12 Receptor β1 Deficiency
来源期刊：Journal of Clinical ImmunologyDOI：10.1007/s10875-019-00637-0
STK4 Deficiency in a Patient with Immune Complex Glomerulonephritis, Salt-Losing Tubulopathy, and Castleman’s-Like Disease
来源期刊：Journal of Clinical ImmunologyDOI：10.1007/s10875-019-00682-9
Successful Rituximab Treatment for Lymphoma, Secondary Immunodeficiency Causing Debilitating Sinusitis: Underlying Primary Immunodeficiency Disease, and Alternative Treatments to Improve the Quality of Life?
来源期刊：Journal of Clinical ImmunologyDOI：10.1007/s10875-019-00636-1
A Novel FOXN1 Variant Is Identified in Two Siblings with Nude Severe Combined Immunodeficiency
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Health-Related Quality of Life and Emotional Health in X-Linked Carriers of Chronic Granulomatous Disease in the United Kingdom
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Compound Heterozygous DOCK8 Mutations in a Patient with B Lymphoblastic Leukemia and EBV-Associated Diffuse Large B Cell Lymphoma
来源期刊：Journal of Clinical ImmunologyDOI：10.1007/s10875-019-00663-y
Neurological Involvement in Childhood Evans Syndrome
来源期刊：Journal of Clinical ImmunologyDOI：10.1007/s10875-019-0594-3
The Value of Chromosome Analysis to Interrogate Variants in DNMT3B Causing Immunodeficiency, Centromeric Instability, and Facial Anomaly Syndrome Type I (ICF1)
来源期刊：Journal of Clinical ImmunologyDOI：10.1007/s10875-019-00704-6
Altered Monocyte Subsets in Patients with Chronic Idiopathic Neutropenia
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BCG Moreau Vaccine Safety Profile and NK Cells—Double Protection Against Disseminated BCG Infection in Retrospective Study of BCG Vaccination in 52 Polish Children with Severe Combined Immunodeficiency
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Compound Heterozygous PGM3 Mutations in a Thai Patient with a Specific Antibody Deficiency Requiring Monthly IVIG Infusions
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Current Status of the Management of Mendelian Susceptibility to Mycobacterial Disease in Mainland China
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Severe Transitory Neonatal Neutropenia Associated with Maternal Autoimmune or Idiopathic Neutropenia
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A Large Cohort of RAG1/2-Deficient SCID Patients—Clinical, Immunological, and Prognostic Analysis
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Successful Lung Transplantation in a Patient with Chronic Granulomatous Disease
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Novel Missense Mutation inSP110Associated with Combined Immunodeficiency and Advanced Liver Disease Without VOD
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Provider Perceptions of Quality of Life, Neurocognition, Physical Well-being, and Psychosocial Health in Patients with Primary Immunodeficiency/Immune Dysregulation Conditions
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Successful Treatment of a Patient with Chronic Systemic Capillary Leak Syndrome, Neutropenia and Thymoma
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Autoinflammation with Infantile Enterocolitis Associated with Recurrent Perianal Abscesses
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Autoinflammation Masquerading as Autoimmunity in an Adult with Heterozygous p.E250K PSTPIP1 Mutation
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RNAseq Supports the Molecular Genetic Diagnosis of Late-Onset ADA Deficiency
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Serum Tryptase Cannot Differentiate Vancomycin-Induced Anaphylaxis From Red Man Syndrome
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The Broad Clinical Spectrum and Transplant Results of PNP Deficiency
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A 1-Year Prospective French Nationwide Study of Emergency Hospital Admissions in Children and Adults with Primary Immunodeficiency
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Disseminated Mycobacterial Disease in a Patient with 22q11.2 Deletion Syndrome: Case Report and Review of the Literature
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Autoimmune Lymphoproliferative Syndrome with Cryptococcus Infection
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RNASEH2B Related Adult-Onset Interferonopathy
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学科领域：医学
影响因子：3.2
中科院分区： 2区
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学科领域：医学
影响因子：3.9
中科院分区： 2区
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影响因子：3.8
中科院分区： 2区
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学科领域：医学
影响因子：3.1
中科院分区： 2区
论文发表 2-4个月录用 7500+文章录用 不成功可退款
新
2026年3月发布
大类学科小类学科Top期刊综述期刊
医学2区
IMMUNOLOGY 免疫学
2区
否
N/A
2025年3月升级版
大类学科小类学科Top期刊综述期刊
医学2区
IMMUNOLOGY 免疫学
2区
否
否
2023年12月旧的升级版
大类学科小类学科Top期刊综述期刊
医学2区
IMMUNOLOGY 免疫学
2区
否
否