Journal of Immunology and Geriatrics

Journal of Immunology and Geriatrics

Journal of Immunology and Geriatrics – Aim And Scope

Open Access & Peer-Reviewed

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Aims & Scope

Journal of Immunology and Geriatrics (JIG) publishes mechanistic research on age-related immune dysfunction, focusing on molecular pathways, biomarkers, and pathophysiological mechanisms underlying immunosenescence and age-associated immune disorders.

Immunosenescence Inflammaging T-cell Exhaustion Autoimmune Pathogenesis Molecular Biomarkers
⚠ Scope Boundary: We do NOT consider clinical management protocols, treatment guidelines, patient care strategies, or therapeutic outcomes without mechanistic investigation.

Tiered Research Scope

Tier 1: Core Domains

Immunosenescence Mechanisms

  • Thymic involution and T-cell repertoire contraction
  • B-cell dysfunction and antibody response decline
  • NK cell senescence and cytotoxicity alterations
  • Myeloid cell polarization in aging
  • Telomere dynamics in immune cells
  • Epigenetic modifications in aged lymphocytes

Typical Fit Example:

"Transcriptomic profiling reveals age-dependent upregulation of PD-1 pathway genes in CD8+ T cells, correlating with reduced cytokine production capacity."

Inflammaging & Chronic Inflammation

  • SASP (senescence-associated secretory phenotype) mediators
  • NF-κB pathway dysregulation in aging
  • Inflammasome activation mechanisms
  • Cytokine network alterations (IL-6, TNF-α, IL-1β)
  • Mitochondrial dysfunction and oxidative stress
  • Cellular senescence markers and pathways

Typical Fit Example:

"NLRP3 inflammasome priming in aged macrophages: role of mtDNA release and cGAS-STING pathway activation."

Autoimmunity Pathogenesis in Aging

  • Loss of central and peripheral tolerance mechanisms
  • Autoreactive T-cell escape and clonal expansion
  • B-cell receptor editing defects
  • Molecular mimicry and epitope spreading
  • Regulatory T-cell dysfunction in elderly
  • Autoantibody production pathways

Typical Fit Example:

"Age-dependent decline in AIRE expression correlates with breakdown of central tolerance and emergence of tissue-specific autoantibodies."

Infectious Disease Susceptibility

  • Pathogen recognition receptor (PRR) signaling defects
  • Impaired antigen presentation in aged APCs
  • Vaccine response mechanisms and failure modes
  • Memory T-cell and B-cell generation deficits
  • Innate immune exhaustion pathways
  • Host-pathogen interaction alterations

Typical Fit Example:

"TLR7/8 signaling attenuation in aged plasmacytoid dendritic cells reduces type I interferon production during influenza infection."

Tier 2: Secondary Focus Areas

Immunogenetics & Molecular Immunology

HLA polymorphisms, immune gene expression profiling, single-cell transcriptomics, genetic susceptibility loci, somatic mutations in immune cells.

Biomarker Discovery

Circulating immune markers, proteomic signatures, metabolomic profiling, immune cell phenotyping, predictive biomarkers for immune aging.

Disease Models & Methodologies

Aged animal models, in vitro senescence systems, organoid technologies, imaging techniques for immune cell tracking, novel immunoassays.

Transplantation Immunology

Allograft rejection mechanisms in elderly, age-related tolerance induction, immunosuppression pharmacodynamics, graft-versus-host disease pathways.

Cancer Immunology in Aging

Immune surveillance decline, tumor microenvironment alterations, checkpoint molecule expression, CAR-T cell dysfunction mechanisms, age-related immunoediting.

Musculoskeletal Immunopathology

Osteoclast-osteoblast signaling, inflammatory mediators in osteoporosis, cartilage degradation pathways, synovial inflammation mechanisms, bone marrow niche alterations.

Tier 3: Emerging & Selective Areas

Computational Immunology

Machine learning for immune cell classification, network analysis of cytokine interactions, predictive modeling of immune aging trajectories. Note: AI/ML applications must directly address immunological mechanisms.

Microbiome-Immune Axis

Gut dysbiosis effects on systemic immunity, microbial metabolite signaling, age-related barrier dysfunction, host-microbe molecular crosstalk.

Neuroimmune Interactions

Microglial activation pathways, neuroinflammation mediators, blood-brain barrier immune cell trafficking, peripheral immune contributions to neurodegeneration.

Regenerative Immunology

Immune cell rejuvenation mechanisms, senolytic compound effects on immune function, stem cell niche immune regulation, tissue repair signaling pathways.

Editorial Note: Tier 3 submissions undergo additional editorial review to ensure mechanistic depth and alignment with pathophysiology focus. Purely descriptive or correlative studies may be declined.

Explicit Exclusions

Out of Scope

Clinical Treatment Protocols

Drug dosing regimens, treatment guidelines, therapeutic algorithms, patient management strategies. Rationale: Focus is on disease mechanisms, not clinical practice.

Clinical Outcomes Research

Mortality rates, hospital readmissions, quality-of-life measures, healthcare utilization without mechanistic investigation. Rationale: Pathophysiology journal, not clinical outcomes.

Diagnostic Criteria & Screening

Diagnostic algorithms, screening protocols, clinical assessment tools without biomarker validation. Rationale: Diagnosis is clinical domain; we focus on underlying pathology.

Health Services & Policy Research

Healthcare delivery models, cost-effectiveness analyses, public health interventions, health economics. Rationale: Outside pathophysiology scope.

Purely Epidemiological Studies

Disease prevalence, incidence rates, risk factor associations without mechanistic exploration. Rationale: Descriptive epidemiology lacks pathophysiological insight.

Behavioral & Psychosocial Research

Cognitive assessments, psychological interventions, social determinants without immune mechanism linkage. Rationale: Must demonstrate direct immunological pathways.

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Article Types & Priorities

Priority 1: Fast-Track

Expedited Review (14-21 days)

Priority 2: Standard

Regular Review (28-35 days)

Priority 3: Selective

Rarely Considered

Editorial Standards & Requirements

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Reporting Guidelines

ARRIVE (animal studies), MIQE (qPCR), MIAME (microarray), STROBE (observational), PRISMA (reviews)

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Data Transparency

Raw data deposition required (GEO, ArrayExpress, Dryad). Code availability for computational analyses. Reagent sharing agreements.

Ethics Compliance

IRB/IACUC approval mandatory. Informed consent documentation. Declaration of Helsinki adherence. GDPR compliance for human data.

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Preprint Policy

Preprints encouraged (bioRxiv, medRxiv). No impact on submission. Must declare preprint DOI. Version control maintained.

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Reproducibility

Detailed methods sections. Antibody validation (CiteAb). Cell line authentication. Statistical power calculations required.

Conflict of Interest

ICMJE disclosure forms. Funding source transparency. Industry collaboration declaration. Competing interests statement.

Decision Metrics & Performance

21
Days to First Decision
32%
Acceptance Rate
45
Days to Publication
Open
Access Model (APC-based)
Before You Submit: Review our scope carefully. Manuscripts outside the defined boundaries will be desk-rejected without review. If uncertain about fit, contact the editorial office with a pre-submission inquiry including title, abstract, and 3-5 keywords. Response within 5 business days.