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Innate immunesenescence: underlying mechanisms and clinical relevance

https://doi.org/10.1007/s10522-014-9514-3
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/1521-4141(200206)32:6<1524::aid-immu1524>3.0.co;2-eopenalex-snapshot
Chemokine production by natural killer cells from nonagenarians
inferredcites →https://doi.org/10.1002/ijc.20998openalex-snapshot
Peripheral blood IFN‐γ‐secreting Vα24 + Vβ11 + NKT cell numbers are decreased in cancer patients independent of tumor type or tumor load
inferredcites →https://doi.org/10.1002/jlb.67.1.40openalex-snapshot
Effect of age on human neutrophil function
inferredcites →https://doi.org/10.1006/cimm.1994.1112openalex-snapshot
Effects of Aging on Natural Killer Cell Activity and Activation by Interleukin-2 and IFN-α
inferredcites →https://doi.org/10.1006/clin.1997.4401openalex-snapshot
Natural Killer Cells in the Late Decades of Human Life
inferredcites →https://doi.org/10.1007/s10522-006-9063-5openalex-snapshot
Decreased frequency and proliferative response of invariant Vα24Vβ11 natural killer T (iNKT) cells in healthy elderly
inferredcites →https://doi.org/10.1007/s10875-010-9448-8openalex-snapshot
Impaired Functions of Peripheral Blood Monocyte Subpopulations in Aged Humans
inferredcites →https://doi.org/10.1007/s11357-010-9191-3openalex-snapshot
Age-associated impaired plasmacytoid dendritic cell functions lead to decreased CD4 and CD8 T cell immunity
inferredcites →https://doi.org/10.1007/s12026-012-8297-3openalex-snapshot
The three human monocyte subsets: implications for health and disease
inferredcites →https://doi.org/10.1016/0002-9343(91)90384-aopenalex-snapshot
Nosocomial infections in elderly patients in the United States, 1986–1990
inferredcites →https://doi.org/10.1016/0024-3205(89)90482-7openalex-snapshot
Neutrophil chemotaxis, phagocytosis and parameters of reactive oxygen species in human aging: Cross-sectional and longitudinal studies
inferredcites →https://doi.org/10.1016/0047-6374(85)90096-xopenalex-snapshot
Age-associated decline in natural killer (NK) activity reflects primarily a defect in function of NK cells
inferredcites →https://doi.org/10.1016/0047-6374(94)90080-9openalex-snapshot
Decline in natural killer cell-mediated immunosurveillance in aging mice — a consequence of reduced cell production and tumor binding capacity
inferredcites →https://doi.org/10.1016/0047-6374(95)01638-4openalex-snapshot
Cytokine production and lymphocyte subpopulations in aged humans. An assessment during nocturnal sleep
inferredcites →https://doi.org/10.1016/0165-2478(96)02519-9openalex-snapshot
Cytokine sensitivity of human NK cells during immunosenescence. 2. IL2-induced Interferon gamma secretion
inferredcites →https://doi.org/10.1016/j.archoralbio.2006.06.008openalex-snapshot
Deterioration of the Langerhans cell network of the human gingival epithelium with aging
inferredcites →https://doi.org/10.1016/j.arr.2003.08.003openalex-snapshot
Skin infections and ageing
inferredcites →https://doi.org/10.1016/j.arr.2013.04.003openalex-snapshot
The impact of ageing on natural killer cell function and potential consequences for health in older adults
inferredcites →https://doi.org/10.1016/j.clim.2006.09.012openalex-snapshot
Peripheral blood dendritic cells and monocytes are differently regulated in the elderly
inferredcites →https://doi.org/10.1016/j.exger.2004.08.005openalex-snapshot
Immunomodulating effect of influenza vaccination in the elderly differing in health status
inferredcites →https://doi.org/10.1016/j.exger.2007.01.009openalex-snapshot
Aging is associated with a rapid decline in frequency, alterations in subset composition, and enhanced Th2 response in CD1d-restricted NKT cells from human peripheral blood
inferredcites →https://doi.org/10.1016/j.exger.2007.05.010openalex-snapshot
Reduced numbers of plasmacytoid dendritic cells in aged blood donors
inferredcites →https://doi.org/10.1016/j.exger.2008.05.016openalex-snapshot
Innate immunity and aging
inferredcites →https://doi.org/10.1016/j.febslet.2007.02.029openalex-snapshot
Effects of aging on triggering receptor expressed on myeloid cells (TREM)‐1‐induced PMN functions
inferredcites →https://doi.org/10.1016/j.humimm.2009.07.005openalex-snapshot
Aging is associated with a numerical and functional decline in plasmacytoid dendritic cells, whereas myeloid dendritic cells are relatively unaltered in human peripheral blood
inferredcites →https://doi.org/10.1016/j.humimm.2010.03.014openalex-snapshot
Variation of human natural killer cell phenotypes with age: Identification of a unique KLRG1-negative subset
inferredcites →https://doi.org/10.1016/j.humimm.2011.01.009openalex-snapshot
Age-related changes in natural killer cell receptors from childhood through old age
inferredcites →https://doi.org/10.1016/j.mad.2005.01.004openalex-snapshot
Reciprocal age related change in natural killer cell receptors for MHC class I
inferredcites →https://doi.org/10.1016/j.mad.2011.08.005openalex-snapshot
Natural killer cell function is altered during the primary response of aged mice to influenza infection
inferredcites →https://doi.org/10.1016/j.molimm.2004.07.034openalex-snapshot
Activation of NK cell cytotoxicity
inferredcites →https://doi.org/10.1016/j.smim.2012.04.008openalex-snapshot
Innate immunosenescence: Effect of aging on cells and receptors of the innate immune system in humans
inferredcites →https://doi.org/10.1016/j.vaccine.2005.04.018openalex-snapshot
The impact of influenza on the health and health care utilisation of elderly people
inferredcites →https://doi.org/10.1016/j.vaccine.2010.12.121openalex-snapshot
Aging reduces the functionality of anti-pneumococcal antibodies and the killing of Streptococcus pneumoniae by neutrophil phagocytosis
inferredcites →https://doi.org/10.1016/s0047-6374(01)00270-6openalex-snapshot
Different IL-8 production by T and NK lymphocytes in elderly subjects
inferredcites →https://doi.org/10.1016/s0047-6374(85)80026-9openalex-snapshot
Suppression of murine natural killer cell activity by adherent cells from aging mice
inferredcites →https://doi.org/10.1016/s0047-6374(96)01829-5openalex-snapshot
Perforins in human cytolytic cells: the effect of age
inferredcites →https://doi.org/10.1016/s0047-6374(98)00156-0openalex-snapshot
Granulocyte and natural killer activity in the elderly
inferredcites →https://doi.org/10.1016/s0047-6374(99)00091-3openalex-snapshot
Genetic differences in the age-associated decrease in inducibility of natural killer cells by interferon-α/β
inferredcites →https://doi.org/10.1016/s0091-6749(86)80121-xopenalex-snapshot
Human basophil releasability
inferredcites →https://doi.org/10.1016/s0264-410x(99)00494-6openalex-snapshot
Unimpaired dendritic cells can be derived from monocytes in old age and can mobilize residual function in senescent T cells
inferredcites →https://doi.org/10.1016/s0531-5565(01)00186-3openalex-snapshot
Vα24+ NKT cells are decreased in elderly humans
inferredcites →https://doi.org/10.1016/s0531-5565(01)00187-5openalex-snapshot
RANTES and MIP-1α production by T lymphocytes, monocytes and NK cells from nonagenarian subjects
inferredcites →https://doi.org/10.1016/s0531-5565(01)00205-4openalex-snapshot
Immunosenescence of macrophages: reduced MHC class II gene expression
inferredcites →https://doi.org/10.1016/s0531-5565(98)00012-6openalex-snapshot
Age-associated differences in neutrophil oxidative burst (chemiluminescence)
inferredcites →https://doi.org/10.1016/s1471-4906(01)02060-9openalex-snapshot
The biology of human natural killer-cell subsets
inferredcites →https://doi.org/10.1016/s1473-3099(04)00931-4openalex-snapshot
Pneumonia in the very old
inferredcites →https://doi.org/10.1034/j.1600-051x.1999.260901.xopenalex-snapshot
Neutrophil migration, oxidative metabolism and adhesion in early onset periodontitis
inferredcites →https://doi.org/10.1034/j.1600-065x.2000.17712.xopenalex-snapshot
Phosphoinositide 3‐kinase: a key biochemical signal for cell migration in response to chemokines
inferredcites →https://doi.org/10.1038/ni.2096openalex-snapshot
Invariant natural killer T cells recognize glycolipids from pathogenic Gram-positive bacteria
inferredcites →https://doi.org/10.1038/ni1138openalex-snapshot
Induced recruitment of NK cells to lymph nodes provides IFN-γ for TH1 priming
inferredcites →https://doi.org/10.1038/onc.2012.206openalex-snapshot
Granule exocytosis mediates immune surveillance of senescent cells
inferredcites →https://doi.org/10.1042/cs0700059openalex-snapshot
Age-related differences in granulocyte Chemotaxis and degranulation
inferredcites →https://doi.org/10.1046/j.1365-2133.2002.04549.xopenalex-snapshot
Tumour necrosis factor-α-induced migration of human Langerhans cells: the influence of ageing
inferredcites →https://doi.org/10.1046/j.1365-2249.2001.01490.xopenalex-snapshot
Age-related changes in membrane lipid composition, fluidity and respiratory burst in rat peritoneal neutrophils
inferredcites →https://doi.org/10.1046/j.1365-2249.2001.01571.xopenalex-snapshot
Association between natural killer cell activity and infection in immunologically normal elderly people
inferredcites →https://doi.org/10.1046/j.1365-2567.1999.00897.xopenalex-snapshot
Age‐related changes in dermal mast cell prevalence in BALB/c mice: functional importance and correlation with dermal mast cell expression of Kit
inferredcites →https://doi.org/10.1046/j.1365-3083.2002.01148.xopenalex-snapshot
Circulating, Interferon‐Producing Plasmacytoid Dendritic Cells Decline During Human Ageing
inferredcites →https://doi.org/10.1056/nejm198906293202605openalex-snapshot
Severe Herpesvirus Infections in an Adolescent without Natural Killer Cells
inferredcites →https://doi.org/10.1073/pnas.0706832104openalex-snapshot
CD4 + CD25 + Foxp3 + regulatory T cells induce alternative activation of human monocytes/macrophages
inferredcites →https://doi.org/10.1073/pnas.91.23.10854openalex-snapshot
Immune function in mice lacking the perforin gene.
inferredcites →https://doi.org/10.1076/ceyr.19.1.26.5337openalex-snapshot
Complement defects in aged mice compromise phagocytosis of Pseudomonas aeruginosa
inferredcites →https://doi.org/10.1083/jcb.135.5.1249openalex-snapshot
A role for phosphoinositide 3-kinase in the completion of macropinocytosis and phagocytosis by macrophages.
inferredcites →https://doi.org/10.1084/jem.180.4.1427openalex-snapshot
Fc receptor stimulation of phosphatidylinositol 3-kinase in natural killer cells is associated with protein kinase C-independent granule release and cell-mediated cytotoxicity.
inferredcites →https://doi.org/10.1084/jem.20090896openalex-snapshot
Decreased TNF-α synthesis by macrophages restricts cutaneous immunosurveillance by memory CD4+ T cells during aging
inferredcites →https://doi.org/10.1084/jem.20100282openalex-snapshot
Age-dependent susceptibility to a viral disease due to decreased natural killer cell numbers and trafficking
inferredcites →https://doi.org/10.1086/516788openalex-snapshot
Prevaccine Determination of the Expression of Costimulatory B7 Molecules in Activated Monocytes Predicts Influenza Vaccine Responses in Young and Older Adults
inferredcites →https://doi.org/10.1089/jir.2011.0058openalex-snapshot
Advanced Age Impairs Macrophage Polarization
inferredcites →https://doi.org/10.1093/gerona/54.4.b150openalex-snapshot
C4, BF, C3 Allele Distribution and Complement Activity in Healthy Aged People and Centenarians
inferredcites →https://doi.org/10.1093/geronj/45.2.m55openalex-snapshot
Neutrophil Function in Healthy Elderly Subjects
inferredcites →https://doi.org/10.1093/intimm/10.7.981openalex-snapshot
Age-dependent decreases of NK cell phosphoinositide turnover during spontaneous but not Fc-mediated cytolytic activity
inferredcites →https://doi.org/10.1111/1523-1747.ep12532761openalex-snapshot
Structural Changes in Aging Human Skin
inferredcites →https://doi.org/10.1111/j.1365-2222.1982.tb01645.xopenalex-snapshot
Skin reactivity, basophil degranulation and IgE levels in ageing
inferredcites →https://doi.org/10.1111/j.1365-2567.2007.02555.xopenalex-snapshot
Immunosenescence: emerging challenges for an ageing population
inferredcites →https://doi.org/10.1111/j.1365-2567.2007.02573.xopenalex-snapshot
In vivo kinetics of human natural killer cells: the effects of ageing and acute and chronic viral infection
inferredcites →https://doi.org/10.1111/j.1474-9726.2005.00178.xopenalex-snapshot
Raised cortisol:DHEAS ratios in the elderly after injury: potential impact upon neutrophil function and immunity
inferredcites →https://doi.org/10.1111/j.1474-9726.2010.00584.xopenalex-snapshot
Human NK cells display major phenotypic and functional changes over the life span
inferredcites →https://doi.org/10.1111/j.1474-9726.2011.00759.xopenalex-snapshot
Age‐associated elevation in TLR5 leads to increased inflammatory responses in the elderly
inferredcites →https://doi.org/10.1111/j.1474-9726.2012.00839.xopenalex-snapshot
Reduced release and binding of perforin at the immunological synapse underlies the age‐related decline in natural killer cell cytotoxicity
inferredcites →https://doi.org/10.1111/j.1474-9726.2012.00851.xopenalex-snapshot
Aging is associated with chronic innate immune activation and dysregulation of monocyte phenotype and function
inferredcites →https://doi.org/10.1111/j.1474-9728.2004.00102.xopenalex-snapshot
Innate immunity in aging: impact on macrophage function
inferredcites →https://doi.org/10.1111/j.1474-9728.2004.00110.xopenalex-snapshot
Signal transduction and functional changes in neutrophils with aging
inferredcites →https://doi.org/10.1111/j.1532-5415.2008.02018.xopenalex-snapshot
Neutrophils of Centenarians Show Function Levels Similar to Those of Young Adults
inferredcites →https://doi.org/10.1126/science.1092385openalex-snapshot
Neutrophil Extracellular Traps Kill Bacteria
inferredcites →https://doi.org/10.1126/science.278.5343.1626openalex-snapshot
CD1d-Restricted and TCR-Mediated Activation of V α 14 NKT Cells by Glycosylceramides
inferredcites →https://doi.org/10.1136/gut.33.7.882openalex-snapshot
Immunosenescence and mucosal immunity: significant effects of old age on secretory IgA concentrations and intraepithelial lymphocyte counts.
inferredcites →https://doi.org/10.1146/annurev-immunol-030409-101305openalex-snapshot
An Integrated View of Humoral Innate Immunity: Pentraxins as a Paradigm
inferredcites →https://doi.org/10.1146/annurev.immunol.21.120601.141126openalex-snapshot
Toll-Like Receptors
inferredcites →https://doi.org/10.1146/annurev.immunol.25.022106.141711openalex-snapshot
The Biology of NKT Cells
inferredcites →https://doi.org/10.1158/0008-5472.can-07-5769openalex-snapshot
Impaired Dendritic Cell Function in Aging Leads to Defective Antitumor Immunity
inferredcites →https://doi.org/10.1159/000022009openalex-snapshot
Influence of Age on Oxidative Bursts (Chemiluminescence) of Polymorphonuclear Neutrophil Leukocytes
inferredcites →https://doi.org/10.1159/000053600openalex-snapshot
Atopic Asthma Is Dominant in Elderly Onset Asthmatics: Possibility for an Alteration of Mast Cell Function by Aging through Fc Receptor Expression
inferredcites →https://doi.org/10.1159/000212809openalex-snapshot
Influence of Age on Polymorphonuclear Leukocytes in vitro: Phagocytic Activity in Healthy Human Subjects
inferredcites →https://doi.org/10.1164/ajrccm.163.4.9909121openalex-snapshot
The Effect of Aging on Nasal Mucociliary Clearance, Beat Frequency, and Ultrastructure of Respiratory Cilia
inferredcites →https://doi.org/10.1172/jci11696openalex-snapshot
IFN-γ–dependent transcription of MHC class II IA is impaired in macrophages from aged mice
inferredcites →https://doi.org/10.1172/jci59777openalex-snapshot
Age-related increases in PGD2 expression impair respiratory DC migration, resulting in diminished T cell responses upon respiratory virus infection in mice
inferredcites →https://doi.org/10.1182/blood-2004-10-4035openalex-snapshot
NK-dependent DC maturation is mediated by TNFα and IFNγ released upon engagement of the NKp30 triggering receptor
inferredcites →https://doi.org/10.1182/blood-2013-08-519520openalex-snapshot
Phosphoinositide 3-kinase inhibition restores neutrophil accuracy in the elderly: toward targeted treatments for immunosenescence
inferredcites →https://doi.org/10.1182/blood.v78.5.1347.1347openalex-snapshot
Effect of age on second messenger generation in neutrophils
inferredcites →https://doi.org/10.1182/blood.v92.7.2410openalex-snapshot
Age-Related Decline of Perforin Expression in Human Cytotoxic T Lymphocytes and Natural Killer Cells
inferredcites →https://doi.org/10.1182/blood.v97.10.3146openalex-snapshot
Human natural killer cells: a unique innate immunoregulatory role for the CD56bright subset
inferredcites →https://doi.org/10.1183/09031936.03.00112302openalex-snapshot
Effect of age and asthma duration upon elastase and α1-antitrypsin levels in adult asthmatics
inferredcites →https://doi.org/10.1183/09031936.05.00002105openalex-snapshot
Long-term clearance from small airways decreases with age
inferredcites →https://doi.org/10.1186/1465-9921-10-112openalex-snapshot
Impaired immune responses in the lungs of aged mice following influenza infection
inferredcites →https://doi.org/10.1186/1471-2172-11-30openalex-snapshot
Age-dependent alterations of monocyte subsets and monocyte-related chemokine pathways in healthy adults
inferredcites →https://doi.org/10.1189/jlb.0106024openalex-snapshot
Molecular basis of age-associated cytokine dysregulation in LPS-stimulated macrophages
inferredcites →https://doi.org/10.1189/jlb.0803389openalex-snapshot
Age-dependent decrease in Toll-like receptor 4-mediated proinflammatory cytokine production and mitogen-activated protein kinase expression
inferredcites →https://doi.org/10.1189/jlb.1007672openalex-snapshot
An age-associated increase in pulmonary inflammation after burn injury is abrogated by CXCR2 inhibition
inferredcites →https://doi.org/10.1189/jlb.70.6.881openalex-snapshot
Senescence in innate immune responses: reduced neutrophil phagocytic capacity and CD16 expression in elderly humans
inferredcites →https://doi.org/10.1371/journal.pone.0041454openalex-snapshot
Innate Immune Dysfunctions in Aged Mice Facilitate the Systemic Dissemination of Methicillin-Resistant S. aureus
inferredcites →https://doi.org/10.1378/chest.07-2114openalex-snapshot
Age-Related Changes in Eosinophil Function in Human Subjects
inferredcites →https://doi.org/10.2177/jsci.3.45openalex-snapshot
A case of κ type IgG multiple myeloma associated with the anti-HBs antibody activity
inferredcites →https://doi.org/10.2741/2692openalex-snapshot
Macrophage activation and polarization
inferredcites →https://doi.org/10.4049/jimmunol.0901022openalex-snapshot
Age-Associated Decrease in TLR Function in Primary Human Dendritic Cells Predicts Influenza Vaccine Response
inferredcites →https://doi.org/10.4049/jimmunol.1002732openalex-snapshot
Human NK Cells Proliferate and Die In Vivo More Rapidly than T Cells in Healthy Young and Elderly Adults
inferredcites →https://doi.org/10.4049/jimmunol.1102002openalex-snapshot
Human NK Cells Induce Neutrophil Apoptosis via an NKp46- and Fas-Dependent Mechanism
inferredcites →https://doi.org/10.4049/jimmunol.1201213openalex-snapshot
Reduced Neutrophil Chemotaxis and Infiltration Contributes to Delayed Resolution of Cutaneous Wound Infection with Advanced Age
inferredcites →https://doi.org/10.4049/jimmunol.154.2.832openalex-snapshot
Antitumoral properties of aged human monocytes.
inferredcites →https://doi.org/10.4049/jimmunol.169.9.4697openalex-snapshot
Cutting Edge: Impaired Toll-Like Receptor Expression and Function in Aging
inferredcites →https://doi.org/10.4049/jimmunol.175.9.5701openalex-snapshot
Age-Induced Reprogramming of Mast Cell Degranulation
inferredcites →https://doi.org/10.4049/jimmunol.178.11.6912openalex-snapshot
Altered Innate Immune Functioning of Dendritic Cells in Elderly Humans: A Role of Phosphoinositide 3-Kinase-Signaling Pathway
inferredcites →https://doi.org/10.4049/jimmunol.178.2.970openalex-snapshot
Age-Associated Defect in Human TLR-1/2 Function
inferredcites →https://doi.org/10.4049/jimmunol.181.5.3156openalex-snapshot
Mononuclear Phagocyte-Derived IL-10 Suppresses the Innate IL-12/IFN-γ Axis in Lung-Challenged Aged Mice

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.3862822openalex-extracted
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inferred← citeshttps://doi.org/10.1002/1873-3468.70215openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/adbi.202200321openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/cmdc.202400672openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/jlb.3mr0822-645rropenalex-snapshot
Immune senescence and periodontitis: From mechanism to therapy
inferred← citeshttps://doi.org/10.1002/mco2.542openalex-snapshot
Cellular senescence in cancer: molecular mechanisms and therapeutic targets
inferred← citeshttps://doi.org/10.1002/mog2.70029openalex-snapshot
Cellular Senescence in Cancer: Mechanisms, Roles in Tumor Progression, and Therapeutic Implications
inferred← citeshttps://doi.org/10.1002/prp2.532openalex-snapshot
Pharmacological plasticity—How do you hit a moving target?
inferred← citeshttps://doi.org/10.1007/978-1-4614-6439-6_101906-1openalex-snapshot
Immunosenescence
inferred← citeshttps://doi.org/10.1007/978-3-030-39903-0_101906openalex-snapshot
Immunosenescence
inferred← citeshttps://doi.org/10.1007/978-3-030-45642-9_13openalex-snapshot
Immunosenescence and CoQ10
inferred← citeshttps://doi.org/10.1007/978-3-030-80038-3_14openalex-snapshot
The Future of Drugs in Sarcopenia
inferred← citeshttps://doi.org/10.1007/978-3-030-87532-9_3openalex-snapshot
Immunesenescence and Compromised Removal of Senescent Cells: Implications for Health in Old Age
inferred← citeshttps://doi.org/10.1007/978-3-030-89162-6_16openalex-snapshot
Frailty Research: The Present and the Future
inferred← citeshttps://doi.org/10.1007/978-3-031-35811-1_9openalex-snapshot
Tailoring Vaccines for Older Individuals: Aging of the Immune System and the Impact on Vaccine Efficacy
inferred← citeshttps://doi.org/10.1007/978-3-319-44870-1_77-1openalex-snapshot
Immunosenescence and Cancer Immunotherapy at Old Age: Basics
inferred← citeshttps://doi.org/10.1007/978-3-319-57415-8_77openalex-snapshot
Immunosenescence and Cancer Immunotherapy at Old Age: Basics
inferred← citeshttps://doi.org/10.1007/978-3-319-64597-1_73-1openalex-snapshot
Assessment of Age-Related Decline of Immunological Function and Possible Methods for Immunological Restoration in Elderly
inferred← citeshttps://doi.org/10.1007/978-3-319-99375-1_73openalex-snapshot
Assessment of Age-Related Decline of Immunological Function and Possible Methods for Immunological Restoration in Elderly
inferred← citeshttps://doi.org/10.1007/978-3-662-53386-4_20-1openalex-snapshot
Sportmedizinische Grundlagen: Immunologische Beanspruchung durch körperliche Belastung
inferred← citeshttps://doi.org/10.1007/978-3-662-53410-6_20openalex-snapshot
Sportmedizinische Grundlagen: Immunologische Beanspruchung durch körperliche Belastung
inferred← citeshttps://doi.org/10.1007/978-981-13-3681-2_3openalex-snapshot
Pulmonary Diseases and Ageing
inferred← citeshttps://doi.org/10.1007/s10096-019-03725-6openalex-snapshot
Cytokine levels predict 30-day mortality in octogenarians and nonagenarians with community-acquired pneumonia: a retrospective observational study
inferred← citeshttps://doi.org/10.1007/s10522-015-9556-1openalex-snapshot
The interconnectedness of ageing: does the convoy principal apply?
inferred← citeshttps://doi.org/10.1007/s10522-018-9774-4openalex-snapshot
Social environment improves immune function and redox state in several organs from prematurely aging female mice and increases their lifespan
inferred← citeshttps://doi.org/10.1007/s11356-023-30148-wopenalex-snapshot
Persistent immune injury induced by short-term decabromodiphenyl ether (BDE-209) exposure to female middle-aged Balb/c mice
inferred← citeshttps://doi.org/10.1007/s11481-020-09947-2openalex-snapshot
Social Environment Ameliorates Behavioral and Immune Impairments in Tyrosine Hydroxylase Haploinsufficient Female Mice
inferred← citeshttps://doi.org/10.1007/s12016-021-08899-6openalex-snapshot
Immunology of Aging: the Birth of Inflammaging
inferred← citeshttps://doi.org/10.1007/s12016-021-08909-7openalex-snapshot
Immunosenescence, Inflammaging, and Frailty: Role of Myeloid Cells in Age-Related Diseases
inferred← citeshttps://doi.org/10.1007/s12603-021-1720-5openalex-snapshot
Interplay between Inflammaging, Frailty and Nutrition in Covid-19: Preventive and Adjuvant Treatment Perspectives
inferred← citeshttps://doi.org/10.1007/s13670-020-00338-2openalex-snapshot
Nutrition and Diabetes in the Context of Inflammaging
inferred← citeshttps://doi.org/10.1007/s40266-025-01210-8openalex-snapshot
Aging in Granulomatosis with Polyangiitis and Microscopic Polyangiitis: From Pathophysiology to Clinical Management
inferred← citeshttps://doi.org/10.1016/b978-0-12-800196-7.00001-3openalex-snapshot
Factors Which Affect the Host Response to Biomaterials
inferred← citeshttps://doi.org/10.1016/b978-0-323-56724-4.00002-2openalex-snapshot
The Inflammatory Response to Surgery
inferred← citeshttps://doi.org/10.1016/b978-0-323-95648-2.00051-4openalex-snapshot
Older subjects and immunogenicity of mRNA COVID-19 vaccines
inferred← citeshttps://doi.org/10.1016/j.ad.2023.05.016openalex-snapshot
Recomendaciones del Grupo de Psoriasis de la Academia Española de Dermatología y Venereología sobre el manejo del paciente de edad avanzada con psoriasis en placas moderada-grave
inferred← citeshttps://doi.org/10.1016/j.ad.2023.07.016openalex-snapshot
[Translated article] Moderate to Severe Psoriasis in Older Adults: Recommendations on Management From the Psoriasis Working Group of the Spanish Academy of Dermatology and Venereology (AEDV)
inferred← citeshttps://doi.org/10.1016/j.arr.2017.01.006openalex-snapshot
Frailty and sarcopenia: The potential role of an aged immune system
inferred← citeshttps://doi.org/10.1016/j.arr.2020.101071openalex-snapshot
The emerging role of T follicular helper (TFH) cells in aging: Influence on the immune frailty
inferred← citeshttps://doi.org/10.1016/j.arr.2025.102870openalex-snapshot
Biomarkers of multimorbidity: A systematic review
inferred← citeshttps://doi.org/10.1016/j.arr.2026.103210openalex-snapshot
Trained immunity in the treatment for haematological malignancy
inferred← citeshttps://doi.org/10.1016/j.arr.2026.103300openalex-snapshot
Thymus regeneration in countering immunosenescence: Mechanisms, strategies and future perspectives
inferred← citeshttps://doi.org/10.1016/j.clnesp.2020.10.003openalex-snapshot
The dietary inflammatory index (DII®) and its association with cognition, frailty, and risk of disabilities in older adults: A systematic review
inferred← citeshttps://doi.org/10.1016/j.healun.2021.04.017openalex-snapshot
Immune response to COVID-19 in older adults
inferred← citeshttps://doi.org/10.1016/j.jneuroim.2020.577240openalex-snapshot
The ratio of prematurely aging to non-prematurely aging mice cohabiting, conditions their behavior, immunity and lifespan
inferred← citeshttps://doi.org/10.1016/j.lfs.2023.122331openalex-snapshot
Vaccine development: Current trends and technologies
inferred← citeshttps://doi.org/10.1016/j.nbd.2022.105721openalex-snapshot
Convergence of signalling pathways in innate immune responses and genetic forms of Parkinson’s disease
inferred← citeshttps://doi.org/10.1016/s1473-3099(21)00460-6openalex-snapshot
Risk factors and disease profile of post-vaccination SARS-CoV-2 infection in UK users of the COVID Symptom Study app: a prospective, community-based, nested, case-control study
inferred← citeshttps://doi.org/10.1038/s12276-024-01287-yopenalex-snapshot
Accelerated aging of skeletal muscle and the immune system in patients with chronic liver disease
inferred← citeshttps://doi.org/10.1038/s41392-025-02145-7openalex-snapshot
Antiageing strategy for neurodegenerative diseases: from mechanisms to clinical advances
inferred← citeshttps://doi.org/10.1038/s41416-020-0986-4openalex-snapshot
Immunotherapy in older patients with non-small cell lung cancer: Young International Society of Geriatric Oncology position paper
inferred← citeshttps://doi.org/10.1038/s41590-017-0006-xopenalex-snapshot
The twilight of immunity: emerging concepts in aging of the immune system
inferred← citeshttps://doi.org/10.1038/s41598-022-23266-xopenalex-snapshot
Influential factors of saliva microbiota composition
inferred← citeshttps://doi.org/10.1038/s43587-024-00644-wopenalex-snapshot
Age differentially impacts adaptive immune responses induced by adenoviral versus mRNA vaccines against COVID-19
inferred← citeshttps://doi.org/10.1089/rej.2018.2164openalex-snapshot
How Could We Slow or Reverse the Human Aging Process and Extend the Healthy Life Span with Heterochronous Autologous Hematopoietic Stem Cell Transplantation
inferred← citeshttps://doi.org/10.1089/vim.2023.0045openalex-snapshot
Immunosenescence and Inflammaging in COVID-19
inferred← citeshttps://doi.org/10.1093/ced/llae347openalex-snapshot
Efficacy and safety of biologics for the treatment of moderate-to-severe psoriasis in older adults: a single-centre Italian experience
inferred← citeshttps://doi.org/10.1093/gerona/glab295openalex-snapshot
Individual Factors Including Age, BMI, and Heritable Factors Underlie Temperature Variation in Sickness and in Health: An Observational, Multi-cohort Study
inferred← citeshttps://doi.org/10.1093/gerona/glw062openalex-snapshot
Reduced Oxidative Burst by Primed Neutrophils in the Elderly Individuals Is Associated With Increased Levels of the CD16bright/CD62LdimImmunosuppressive Subset
inferred← citeshttps://doi.org/10.1111/cei.12851openalex-snapshot
Immune senescence: significance of the stromal microenvironment
inferred← citeshttps://doi.org/10.1111/cei.12876openalex-snapshot
The convergence of senescence and nutrient sensing during lymphocyte ageing
inferred← citeshttps://doi.org/10.1111/cen3.12723openalex-snapshot
Development of infections among patients with myasthenia gravis undergoing immunotherapy
inferred← citeshttps://doi.org/10.1111/ggi.14027openalex-snapshot
Reactive leukocytosis in older patients with acute colonic diverticulitis: A retrospective study utilizing logistic regression analysis
inferred← citeshttps://doi.org/10.1152/ajpcell.00153.2025openalex-snapshot
Metabolic dysregulation of trained immunity in immune aging and the impact of dietary patterns
inferred← citeshttps://doi.org/10.1152/ajpendo.00169.2025openalex-snapshot
Transcriptomic analyses of peripheral blood mononuclear cells reveal age-specific basal and acute exercise responsiveness differences in humans
inferred← citeshttps://doi.org/10.1155/2017/4234765openalex-snapshot
Does Regular Exercise Counter T Cell Immunosenescence Reducing the Risk of Developing Cancer and Promoting Successful Treatment of Malignancies?
inferred← citeshttps://doi.org/10.1159/000484488openalex-snapshot
Erosive Pustular Dermatosis: A Manifestation of Immunosenescence A Report of 8 Cases
inferred← citeshttps://doi.org/10.1177/1203475419897578openalex-snapshot
Biologic Treatment in Elderly Patients With Psoriasis: A Systematic Review
inferred← citeshttps://doi.org/10.1186/s12931-021-01619-wopenalex-snapshot
Asthma in elderly is characterized by increased sputum neutrophils, lower airway caliber variability and air trapping
inferred← citeshttps://doi.org/10.1186/s12979-025-00549-1openalex-snapshot
“Immunopause” no more: exercise to counter immunosenescence in aging
inferred← citeshttps://doi.org/10.1186/s13045-020-00986-zopenalex-snapshot
Immunosenescence: a key player in cancer development
inferred← citeshttps://doi.org/10.1186/s13075-018-1624-xopenalex-snapshot
Ten weeks of high-intensity interval walk training is associated with reduced disease activity and improved innate immune function in older adults with rheumatoid arthritis: a pilot study
inferred← citeshttps://doi.org/10.1186/s13102-024-00890-wopenalex-snapshot
The chronic leukocyte and inflammatory cytokine responses of older adults to resistance training in normobaric hypoxia; a randomized controlled trial
inferred← citeshttps://doi.org/10.14302/issn.2474-7785.jarh-17-1578openalex-snapshot
Frailty and the Immune System
inferred← citeshttps://doi.org/10.1634/theoncologist.2016-0276openalex-snapshot
Management of Cancer in the Older Age Person: An Approach to Complex Medical Decisions
inferred← citeshttps://doi.org/10.18632/aging.203689openalex-snapshot
Restoration of aged hematopoietic cells by their young counterparts through instructive microvesicles release
inferred← citeshttps://doi.org/10.21037/atm-22-1592openalex-snapshot
Screening of periodontitis-related genes and immune cells based on an integrated bioinformatics analysis
inferred← citeshttps://doi.org/10.3389/fcimb.2023.1229098openalex-snapshot
Contribution of viral and bacterial infections to senescence and immunosenescence
inferred← citeshttps://doi.org/10.3389/fendo.2026.1917096openalex-snapshot
Senescent immune cells, inflammaging, and bone loss: therapeutic potential and translational challenges of senolytics in osteoporosis
inferred← citeshttps://doi.org/10.3389/fimmu.2018.00648openalex-snapshot
Debunking the Myth of Exercise-Induced Immune Suppression: Redefining the Impact of Exercise on Immunological Health Across the Lifespan
inferred← citeshttps://doi.org/10.3389/fimmu.2020.00729openalex-snapshot
Rejuvenation of Neutrophil Functions in Association With Reduced Diabetes Risk Following Ten Weeks of Low-Volume High Intensity Interval Walking in Older Adults With Prediabetes – A Pilot Study
inferred← citeshttps://doi.org/10.3389/fimmu.2020.01748openalex-snapshot
Remodeling of the Immune Response With Aging: Immunosenescence and Its Potential Impact on COVID-19 Immune Response
inferred← citeshttps://doi.org/10.3389/fimmu.2020.583019openalex-snapshot
Targeting Inflammation and Immunosenescence to Improve Vaccine Responses in the Elderly
inferred← citeshttps://doi.org/10.3389/fimmu.2020.583077openalex-snapshot
Emerging Concepts and Technologies in Vaccine Development
inferred← citeshttps://doi.org/10.3389/fimmu.2023.1334205openalex-snapshot
A metabolic perspective of the neutrophil life cycle: new avenues in immunometabolism
inferred← citeshttps://doi.org/10.3389/fimmu.2026.1779141openalex-snapshot
Dual roles of immunosenescence in cancer immunotherapy
inferred← citeshttps://doi.org/10.3389/fragi.2026.1847033openalex-snapshot
Age-associated remodeling of NK cell subsets, B cell subsets, and T cell surface markers in peripheral blood of healthy Chinese adults: a prospective multicolor flow cytometry study
inferred← citeshttps://doi.org/10.3390/biom12101456openalex-snapshot
Immunosenescence, Inflammaging, and Lung Senescence in Asthma in the Elderly
inferred← citeshttps://doi.org/10.3390/cells11010115openalex-snapshot
Exogenous and Endogenous Dendritic Cell-Derived Exosomes: Lessons Learned for Immunotherapy and Disease Pathogenesis
inferred← citeshttps://doi.org/10.3390/cells11233818openalex-snapshot
The DARC Side of Inflamm-Aging: Duffy Antigen Receptor for Chemokines (DARC/ACKR1) as a Potential Biomarker of Aging, Immunosenescence, and Breast Oncogenesis among High-Risk Subpopulations
inferred← citeshttps://doi.org/10.3390/cells14171374openalex-snapshot
Senescent Polarization of Macrophages and Inflammatory Biomarkers in Cardiovascular Disease
inferred← citeshttps://doi.org/10.3390/cells15080657openalex-snapshot
Immunosenescence and Inflammaging as Drivers of Neurodegeneration: Cellular Mechanisms, Neuroimmune Crosstalk, and Therapeutic Implications
inferred← citeshttps://doi.org/10.3390/geriatrics8040079openalex-snapshot
Changes in Interleukin-1β, Tumor Necrosis Factor-α, and Interleukin-10 Cytokines in Older People with Periodontitis
inferred← citeshttps://doi.org/10.3390/ijms20143586openalex-snapshot
Contribution of Aging, Obesity, and Microbiota on Tumor Immunotherapy Efficacy and Toxicity
inferred← citeshttps://doi.org/10.3390/ijms20163878openalex-snapshot
Molecular and Cellular Bases of Immunosenescence, Inflammation, and Cardiovascular Complications Mimicking “Inflammaging” in Patients with Systemic Lupus Erythematosus
inferred← citeshttps://doi.org/10.3390/ijms242316904openalex-snapshot
Energy Regulation in Inflammatory Sarcopenia by the Purinergic System
inferred← citeshttps://doi.org/10.3390/nu13124337openalex-snapshot
Nutrition and Healthy Aging: Prevention and Treatment of Gastrointestinal Diseases
inferred← citeshttps://doi.org/10.3390/nu9030191openalex-snapshot
The Effect of Bifidobacterium animalis ssp. lactis HN019 on Cellular Immune Function in Healthy Elderly Subjects: Systematic Review and Meta-Analysis
inferred← citeshttps://doi.org/10.3390/vaccines11010154openalex-snapshot
Ageing Curtails the Diversity and Functionality of Nascent CD8+ T Cell Responses against SARS-CoV-2
inferred← citeshttps://doi.org/10.36150/2499-6564-n580openalex-snapshot
Healthy aging: when periodontal health matters
inferred← citeshttps://doi.org/10.3889/oamjms.2022.9034openalex-snapshot
The Immunogenicity and Safety of Influenza Vaccines among Indonesian Older adult
inferred← citeshttps://doi.org/10.5937/arhfarm1906469bopenalex-snapshot
Application of prophylactic vaccines in the elderly
inferred← citeshttps://doi.org/10.6084/m9.figshare.25744288openalex-snapshot
Additional file 1 of The chronic leukocyte and inflammatory cytokine responses of older adults to resistance training in normobaric hypoxia; a randomized controlled trial
Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.