The DOI matches its Crossref record; 139 of the 139 references it cites were found in a registry or an index.
Control of adaptive immunity by the innate immune system
Open accessAbstract
Microbial infections are recognized by the innate immune system both to elicit immediate defense and to generate long-lasting adaptive immunity. To detect and respond to vastly different groups of pathogens, the innate immune system uses several recognition systems that rely on sensing common structural and functional features associated with different classes of microorganisms. These recognition systems determine microbial location, viability, replication and pathogenicity. Detection of these features by recognition pathways of the innate immune system is translated into different classes of effector responses though specialized populations of dendritic cells. Multiple mechanisms for the induction of immune responses are variations on a common design principle wherein the cells that sense infections produce one set of cytokines to induce lymphocytes to produce another set of cytokines, which in turn activate effector responses. Here we discuss these emerging principles of innate control of adaptive immunity.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“TLRs do not directly initiate phagocytosis but facilitate it more effectively [27].”
From Insights of Endocytosis Signaling in Health and Disease (2023) · cites this paper as [27]
Experimental — accuracy not yet measuredIn the citing paper
“In more than 400 healthy, middle to early old age participants drawn from the Whitehall II Cohort study, self-reported short sleep duration in men, but not in women, was related to shorter leukocyte telomere length”
From The Sleep-Immune Crosstalk in Health and Disease (2019) · cites this paper as [267]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Neutrophil Extracellular Traps Kill Bacteria
Brinkmann, V., Reichard, U., Goosmann, C., Fauler, B., Uhlemann, Y., Weiss, D. S., Weinrauch, Y., & Zychlinsky, A. (2004) · Science · doi:10.1126/science.1092385 · Cited by 10,268
The role of pattern-recognition receptors in innate immunity: update on Toll-like receptors
Kawai, T., & Akira, S. (2010) · Nature Immunology · doi:10.1038/ni.1863 · Cited by 9,304
Acute-Phase Proteins and Other Systemic Responses to Inflammation
Gabay, C., & Kushner, I. (1999) · New England Journal of Medicine · doi:10.1056/nejm199902113400607 · Cited by 6,734
Origin and physiological roles of inflammation
Medzhitov, R. (2008) · Nature · doi:10.1038/nature07201 · Cited by 6,618
Self-citationKorn, T., Bettelli, E., Oukka, M., & Kuchroo, V. K. (2009) · Annual Review of Immunology · doi:10.1146/annurev.immunol.021908.132710 · Cited by 4,873
Macrophage biology in development, homeostasis and disease
Wynn, T. A., Chawla, A., & Pollard, J. W. (2013) · Nature · doi:10.1038/nature12034 · Cited by 4,684
Plant pathogens and integrated defence responses to infection
Dangl, J. L., & Jones, J. D. G. (2001) · Nature · doi:10.1038/35081161 · Cited by 3,959
Approaching the asymptote? Evolution and revolution in immunology.Preprint
Janeway, C. (1989) · Cold Spring Harbor Symposia on Quantitative Biology · doi:10.1101/sqb.1989.054.01.003 · Cited by 3,396
Cryopyrin activates the inflammasome in response to toxins and ATP
Mariathasan, S., Weiss, D. S., Newton, K., McBride, J., O'Rourke, K., Roose-Girma, M., Lee, W. P., Weinrauch, Y., Monack, D. M., & Dixit, V. M. (2006) · Nature · doi:10.1038/nature04515 · Cited by 3,080
Development of Monocytes, Macrophages, and Dendritic Cells
Geissmann, F., Manz, M. G., Jung, S., Sieweke, M. H., Merad, M., & Ley, K. (2010) · Science · doi:10.1126/science.1178331 · Cited by 3,049
Flagged first, then by citations
Cited by
Sorted by citations
Items 501–600 of 1,003
Lieber, C. M., Aggarwal, M., Yoon, J.-J., Cox, R. M., Sourimant, J., Toots, M., Kang, H., Johnson, S. K., Jones, C. A., Sticher, Z. M., et al. (2023) · PLoS Pathogens · doi:10.1371/journal.ppat.1011342 · Cited by 42
“Although essentially sterilizing, even prophylactic treatment resulted in partial protection of animals at re-infection despite the absence of neutralizing antibodies, indicating that treated animals also mounted a viable cell-mediated adaptive response [48,49].”
BackgroundIntensive care management of acute-on-chronic liver failure
Perricone, G., Artzner, T., Martin, E. D., Jalan, R., Wendon, J. A., & Carbone, M. (2023) · Intensive Care Medicine · doi:10.1007/s00134-023-07149-x · Cited by 42
Immune cell-derived exosomes as promising tools for cancer therapy
Chen, J., Zhang, G., Wan, Y., Xia, B., Ni, Q., Shan, S., Hu, Z., & Liang, X. (2023) · Journal of Controlled Release · doi:10.1016/j.jconrel.2023.11.003 · Cited by 46
A TRAF3-NIK module differentially regulates DNA vs RNA pathways in innate immune signaling
Parvatiyar, K., Pindado, J., Dev, A., Aliyari, S. R., Zaver, S. A., Gerami, H., Chapon, M., Ghaffari, A. A., Dhingra, A., & Cheng, G. (2018) · Nature Communications · doi:10.1038/s41467-018-05168-7 · Cited by 43
Warnecke, A., Prenzler, N., Schmitt, H., Daemen, K., Keil, J., Dursin, M., Lenarz, T., & Falk, C. S. (2019) · Frontiers in Neurology · doi:10.3389/fneur.2019.00665 · Cited by 42
“, peptides in the context of major histocompatibility complex (MHC), particularly by dendritic cells (12).”
BackgroundNucleic acid-based therapy for coronavirus disease 2019
Piyush, R., Rajarshi, K., Chatterjee, A., Khan, R., & Ray, S. (2020) · Heliyon · doi:10.1016/j.heliyon.2020.e05007 · Cited by 44
“Various pattern recognition receptors (PRRs) like TLR3, TLR7, and TLR8 situated in endosomes and MDA-5, PKR, RIG-I, NLRP3, and NOD-2 present in the cytoplasm of mammalian cells assist in sensing the foreign RNA [68, 69, 70].”
Kim, H., Lee, S., & Ki, C. S. (2020) · Carbohydrate Polymers · doi:10.1016/j.carbpol.2020.117132 · Cited by 42
Nanomaterials-Mediated Immunomodulation for Cancer Therapeutics
Jindal, A., Sarkar, S., & Alam, A. (2021) · Frontiers in Chemistry · doi:10.3389/fchem.2021.629635 · Cited by 42
“Such responses lack specificity but act as a fast and effective primary response against foreign particles (Turvey and Broide, 2010; Iwasaki and Medzhitov, 2015).”
BackgroundThe role of dendritic cells in allergic diseases
Liu, P., Kang, C., Zhang, J., Liu, Y., Liu, J., Hu, T., Zeng, X., & Qiu, S. (2022) · International Immunopharmacology · doi:10.1016/j.intimp.2022.109449 · Cited by 40
Novel long non-coding RNAs associated with inflammation and macrophage activation in human
Chini, A., Guha, P., Malladi, V. S., Guo, Z., & Mandal, S. S. (2023) · Scientific Reports · doi:10.1038/s41598-023-30568-1 · Cited by 44
Roles for Siglec-glycan interactions in regulating immune cells
Lin, S.-Y., Schmidt, E. N., Takahashi, K., & Macauley, M. S. (2024) · Seminars in Immunology · doi:10.1016/j.smim.2024.101925 · Cited by 40
Tsai, W.-T., Lo, Y.-C., Wu, M.-S., Li, C., Kuo, Y.-P., Lai, Y.-H., Tsai, Y., Chen, K.-C., Chuang, T., Yao, C.-H., et al. (2016) · Journal of Biological Chemistry · doi:10.1074/jbc.m115.686683 · Cited by 42
“Innate immune responses are important for pathogen elimination and the activation of adaptive immune responses (1).”
BackgroundEffects of sodium fluoride on blood cellular and humoral immunity in mice
Guo, H., Kuang, P., Luo, Q., Cui, H., Deng, H., Liu, H., Lu, Y., Fang, J. S., Zuo, Z., Deng, J., et al. (2017) · Oncotarget · doi:10.18632/oncotarget.20198 · Cited by 41
“The adaptive immune system includes T and B lymphocytes, specific antibodies, cytokines and chemokines [39].”
BackgroundLǐ, Y., Shang, P., Shyu, D.-L., Carrillo, C., Naraghi‐Arani, P., Jaing, C. J., Renukaradhya, G. J., Firth, A. E., Snijder, E. J., & Fāng, Y. (2018) · Virology · doi:10.1016/j.virol.2017.12.017 · Cited by 41
“A strong innate immune response following a viral infection is expected to enhance the cell-mediated adaptive immunity (Iwasaki and Medzhitov, 2015; Jain and Pasare, 2017).”
BackgroundImmunostimulation and Immunosuppression: Nanotechnology on the Brink
Fontana, F., Figueiredo, P., Bauleth‐Ramos, T., Correia, A., & Santos, H. A. (2018) · Small Methods · doi:10.1002/smtd.201700347 · Cited by 41
Immune Ecosystem of Virus-Infected Host Tissues
Maarouf, M., Rai, K. R., Goraya, M. U., & Chen, J. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19051379 · Cited by 41
“The cellular immunity is driven by α-β T cell receptors expressed by T lymphocytes that recognize the antigen processed peptide bound to MHC molecules on the surface of infected cells [134,135].”
BackgroundNucleic acids presenting polymer nanomaterials as vaccine adjuvants
Comberlato, A., Paloja, K., & Bastings, M. M. C. (2019) · Journal of Materials Chemistry B · doi:10.1039/c9tb01222b · Cited by 39
Lung Microbiome Participation in Local Immune Response Regulation in Respiratory Diseases
Lira-Lucio, J. A., Falfán‐Valencia, R., Ramírez‐Venegas, A., Buendía-Roldán, I., Rojas‐Serrano, J., Mejía, M. E., & Pérez-Rubio, G. (2020) · Microorganisms · doi:10.3390/microorganisms8071059 · Cited by 45
“Type 3 immunity integrates RORγt+ lymphocytes that produce IL-17A, IL7F, IL-22, and IL-26, and this pathway is activated in the presence of bacteria or extracellular fungi [32,33].”
BackgroundZheng, K., Wu, S., Lv, Y., Pang, P., Deng, L., Xu, H., Shi, Y., & Chen, X. (2020) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2020.113555 · Cited by 41
Chatterjee, B., Sandhu, H. S., & Dixit, N. M. (2022) · PLoS Pathogens · doi:10.1371/journal.ppat.1010630 · Cited by 41
Translating musculoskeletal bioengineering into tissue regeneration therapies
Khodabukus, A., Guyer, T., Moore, A. C., Stevens, M. M., Guldberg, R. E., & Bursac, N. (2022) · Science Translational Medicine · doi:10.1126/scitranslmed.abn9074 · Cited by 40
“Regeneration is initiated by the release of damage-associated molecular pattern molecules (DAMPs), chemokines, and lipid mediators from damaged cells to recruit neutrophils, monocytes/macrophages, and T lymphocytes to the injury site (11).”
BackgroundWolf, L., Sapich, S., Honecker, A., Jungnickel, C., Seiler, F., Bischoff, M., Wonnenberg, B., Herr, C., Schneider‐Daum, N., Lehr, C., et al. (2016) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.00158.2016 · Cited by 40
“Lung epithelial cells are suggested to contribute to pathogeninduced inflammation by detecting microbes with patternrecognition receptors (PRR) resulting in enhanced chemokinemediated recruitment of circulating leukocytes (13, 28).”
BackgroundMicrobiota induces tonic CCL2 systemic levels that control pDC trafficking in steady state
Swiecki, M. K., Miller, H. L., Sesti‐Costa, R., Cella, M., Gilfillan, S., & Colonna, M. (2016) · Mucosal Immunology · doi:10.1038/mi.2016.99 · Cited by 38
Koppenol-Raab, M., Sjoelund, V. H., Manes, N. P., Gottschalk, R. A., Dutta, B., Benet, Z. L., Fraser, I. D. C., & Nita‐Lazar, A. (2017) · Molecular & Cellular Proteomics · doi:10.1074/mcp.m116.064261 · Cited by 42
“The innate immune system is essential for host defense, providing a rapid initial reaction to infection or tissue damage and activating adaptive immunity (1).”
BackgroundMethodBenchmarking the HLA typing performance of Polysolver and Optitype in 50 Danish parental trios
Matey-Hernandez, M. L., Brunak, S., & Izarzugaza, J. M. G. (2018) · BMC Bioinformatics · doi:10.1186/s12859-018-2239-6 · Cited by 41
Ubiquitination and phosphorylation of the CARD11-BCL10-MALT1 signalosome in T cells
Lork, M., Staal, J., & Beyaert, R. (2018) · Cellular Immunology · doi:10.1016/j.cellimm.2018.11.001 · Cited by 42
Structure and function of lipid A–modifying enzymes
Anandan, A., & Vrielink, A. (2019) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.14244 · Cited by 40
Type 1 diabetes and engineering enhanced islet transplantation
Jeyagaran, A., Lu, C., Zbinden, A., Birkenfeld, A. L., Brucker, S. Y., & Layland, S. L. (2022) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2022.114481 · Cited by 42
Gautam, S., Kim, T., Lester, E., Deep, D., & Spiegel, D. A. (2015) · ACS Chemical Biology · doi:10.1021/acschembio.5b00439 · Cited by 40
Kiritsy, M. C., Ankley, L. M., Trombley, J. D., Huizinga, G. P., Lord, A. E., Orning, P., Elling, R., Fitzgerald, K. A., & Olive, A. J. (2021) · eLife · doi:10.7554/elife.65110 · Cited by 34
“Activation of the host response to infection requires the coordinated interaction between antigen presenting cells (APCs) and T cells (van Elsland and Neefjes, 2018; Iwasaki and Medzhitov, 2015; Tubo and Jenkins, 2014).”
BackgroundInteraction between alveolar macrophages and epithelial cells during Mycoplasma pneumoniae infection
Xue, Y., Wang, M., & Han, H. (2023) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2023.1052020 · Cited by 42
“Subsequently, there is the recruitment of myeloid cells, such as monocytes (MCS) and neutrophils, which amplifies the inflammatory response for controlling infection (Chaplin, 2010; Iwasaki and Medzhitov, 2015).”
BackgroundGonzalez, A. L., Dungan, M. M., Smart, C. D., Madhur, M. S., & Doran, A. C. (2023) · Antioxidants and Redox Signaling · doi:10.1089/ars.2023.0284 · Cited by 42
“Similarly, when mice are chronically exposed to inflammatory cytokines, such as TNF-a , they develop blunted adaptive immune responses (Cope et al., 1997; Feehan and Gilroy, 2019; Iwasaki and Medzhitov, 2015).”
Natural polysaccharides exert anti-tumor effects as dendritic cell immune enhancers
Xiong, H., Han, X., Cai, L., & Zheng, H. (2023) · Frontiers in Oncology · doi:10.3389/fonc.2023.1274048 · Cited by 40
“If the PRRs on DCs recognize TAAs, then DCs shift gene transcription and cellular metabolism, gradually migrating to lymphoid organs and transforming into mature DCs (51).”
BackgroundRoyal Jelly Fatty Acids: Chemical Composition, Extraction, Biological Activity, and Prospect
Yu, X., Tu, X., Tao, L., Daddam, J. R., Li, S., & Hu, F. (2023) · Journal of Functional Foods · doi:10.1016/j.jff.2023.105868 · Cited by 44
Novel Insights into the Pathogenesis of Hirschsprung's-associated Enterocolitis
Jiao, C., Chen, X., & Feng, J. (2016) · Chinese Medical Journal · doi:10.4103/0366-6999.183433 · Cited by 39
“Besides, macrophages, dendritic cells, innate lymphoid cells, paneth cells found only in the small intestine, goblet cells and intestinal epithelial cells all contribute to intestinal innate immunity and then adaptive immunity.[46-48]”
BackgroundZheng, B., Xu, J., Chen, G., Zhang, S., Xiao, Z., & Lü, W. (2019) · Advanced Functional Materials · doi:10.1002/adfm.201901437 · Cited by 39
Cutting Edge: TAK1 Safeguards Macrophages against Proinflammatory Cell Death
Sanjo, H., Nakayama, J., Yoshizawa, T., Fehling, H. J., Akira, S., & Taki, S. (2019) · The Journal of Immunology · doi:10.4049/jimmunol.1900202 · Cited by 39
“The best-known example of pattern recognition receptors is TLRs, and it is now appreciated that engagement of TLRs triggers inflammatory responses that are essential for the activation of both the innate and adaptive immune systems (5).”
BackgroundA Population of M2 Macrophages Associated With Bone Formation
Olmsted‐Davis, E. A., Mejia, J., Salisbury, E. A., Gugala, Z., & Davis, A. R. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.686769 · Cited by 41
Prockop, D. J., Oh, J. Y., & Lee, R. H. (2017) · Molecular Therapy · doi:10.1016/j.ymthe.2017.06.004 · Cited by 40
“Therefore, as these data were being developed, they suggested the hypothesis that the MSCs primarily affect the innate immune system that controls development of acquired immunity.(33,34) The hypothesis has now been substantiated for both mMSCs and hMSCs by reports by multiple investigators.”
BackgroundCytokine-armed pyroptosis induces antitumor immunity against diverse types of tumors
Orehek, S., Ramuta, T. Ž., Lainšček, D., Malenšek, Š., Šala, M., Benčina, M., Jerala, R., & Hafner‐Bratkovič, I. (2024) · Nature Communications · doi:10.1038/s41467-024-55083-3 · Cited by 41
“The innate immune system with a lineup of genetically encoded pattern recognition receptors provides the fastest response to various types of threats and instructs the development of adaptive immune responses 6 .”
Shin, J., Choi, D.-K., Sohn, K., Kim, S., Ha, J. M., Lee, Y., Im, M., Seo, Y., Kim, C. D., Lee, J., et al. (2017) · Scientific Reports · doi:10.1038/srep44127 · Cited by 38
Shim, J., Lee, H., Park, D.-E., Lee, J., Bae, B., Chang, Y., Kim, J., Kim, H. Y., & Kang, H. (2019) · Allergy · doi:10.1111/all.14017 · Cited by 38
Thwe, P. M., Fritz, D. I., Snyder, J. P., Smith, P. R., Curtis, K. D., O'Donnell, A., Galasso, N. A., Sepaniac, L. A., Adamik, B. J., Hoyt, L. R., et al. (2019) · Journal of Leukocyte Biology · doi:10.1002/jlb.3a0819-207rr · Cited by 38
Mao, R., Wu, L., Zhu, N., Liu, X., Hao, Y., Liu, R., Du, Q., & Li, Y. (2020) · Journal of Functional Foods · doi:10.1016/j.jff.2020.104068 · Cited by 38
Antibacterial activity of human defensins against Staphylococcus aureus and Escherichia coli
Bolatchiev, A. (2020) · PeerJ · doi:10.7717/peerj.10455 · Cited by 39
Reis, P. A., & Castro-Faria-Neto, H. C. (2022) · Frontiers in Neuroscience · doi:10.3389/fnins.2021.742158 · Cited by 40
“Immune cells (especially macrophages and neutrophils) are recruited, increasing the inflammatory response and tissue damage (Lehnardt, 2010; Iwasaki and Medzhitov, 2015; Andreasson et al., 2016).”
BackgroundCirillo, G., Negrete-Diaz, F., Yucumá, D., Virtuoso, A., Korai, S. A., Luca, C. D., Kaniušas, E., Papa, M., & Panetsos, F. (2022) · Cells · doi:10.3390/cells11244103 · Cited by 40
Elahi, S. (2020) · The Journal of Immunology · doi:10.4049/jimmunol.2000710 · Cited by 37
“, a bacterium versus a virus or a fungus) but also selects the immune and energetic cost of its response (72).”
BackgroundInfluentialTENT5 cytoplasmic noncanonical poly(A) polymerases regulate the innate immune response in animals
Liudkovska, V., Krawczyk, P. S., Brouze, A., Gumińska, N., Węgierski, T., Cysewski, D., Mackiewicz, Z., Ewbank, J. J., Drabikowski, K., Mroczek, S., et al. (2022) · Science Advances · doi:10.1126/sciadv.add9468 · Cited by 36
“In mammals, innate immunity functions alongside adaptive immunity and also plays a key role in its activation (2, 3).”
BackgroundMacrophage-derived oncostatin M repairs the lung epithelial barrier during inflammatory damage
Hoagland, D. A., Rodríguez-Morales, P., Mann, A. O., Vazquez, A. Y. B., Yu, S., Lai, A., Kane, H., Dang, S. M., Lin, Y., Thorens, L., et al. (2025) · Science · doi:10.1126/science.adi8828 · Cited by 40
Self-citationQiu, W., Shen, Y., Pan, C., Liu, S., Wu, M., Yang, M., & Wang, K. (2016) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2016.04.015 · Cited by 37
“Complements are essential components of the innate immune system and provide an important link between adaptive and innate immune responses (Iwasaki and Medzhitov, 2015).”
BackgroundInnate sensors that regulate vaccine responses
Georg, P., & Sander, L. E. (2019) · Current Opinion in Immunology · doi:10.1016/j.coi.2019.02.006 · Cited by 36
Poly(I:C) Potentiates T Cell Immunity to a Dendritic Cell Targeted HIV-Multiepitope Vaccine
Apostólico, J. D. S., Lunardelli, V. A. S., Yamamoto, M. M., Cunha‐Neto, E., Boscardin, S. B., & Rosa, D. S. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.00843 · Cited by 37
“DCs express a wide range of receptors including pattern recognition receptors (PRRs), like toll-like receptors (TLRs), cytosolic receptors, and Ctype lectin receptors, that are able to recognize pathogen- or damage- associated molecular patterns (PAMPs or DAMPs, respectively) (3).”
BackgroundThe immunological roles in acute-on-chronic liver failure: An update
Chen, P., Wang, Y., Chen, C., Guan, J., Zhu, H., & Chen, Z. (2019) · Hepatobiliary & pancreatic diseases international · doi:10.1016/j.hbpd.2019.07.003 · Cited by 39
Wood, T. E., Aksoy, E., & Hachani, A. (2020) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2020.587948 · Cited by 40
“Innate immune cells, particularly antigen-presenting dendritic cells (DCs) sense their environment in peripheral organs through continuous uptake and sampling of exogenously acquired antigens (Iwasaki and Medzhitov, 2015).”
BackgroundMolecular adaptations during viral epidemics
Rochman, N. D., Wolf, Y. I., & Koonin, E. V. (2022) · EMBO Reports · doi:10.15252/embr.202255393 · Cited by 38
“Adaptive immune responses are at least in part directed by pathogen-sensing via pattern recognition receptors conducted by the innate immune system (Iwasaki & Medzhitov, 2015), which may be evaded by viruses (Beachboard & Horner, 2016; Kikkert, 2020), undercutting many “downstream” adaptive…”
Chandra, A., Yoon, S., Michieletto, M. F., Goldman, N., Ferrari, E. K., Abedi, M., Johnson, I., Fasolino, M., Pham, K., Joannas, L. D., et al. (2023) · Immunity · doi:10.1016/j.immuni.2023.05.004 · Cited by 39
Primary nasal influenza infection rewires tissue-scale memory response dynamics
Kazer, S. W., Matysiak, C., Langan, E. M., Messou, M.-A., LaSalle, T. J., O’Leary, E., Marbourg, J. M., Naughton, K. A., von Andrian, U. H., & Ordovás-Montañés, J. (2024) · Immunity · doi:10.1016/j.immuni.2024.06.005 · Cited by 39
Emerging biomedical technologies for scarless wound healing
Cao, X., Wu, X., Zhang, Y., Qian, X., Sun, W., & Zhao, Y. (2024) · Bioactive Materials · doi:10.1016/j.bioactmat.2024.09.001 · Cited by 38
“Macrophages provide key signaling molecules involved in wound healing, and their malfunction can lead to increased myofibroblast activation and type I/III collagen deposition, which can interfere with normal regeneration and encourage the onset of fibrosis [54,55].”
Age-associated changes in innate and adaptive immunity: role of the gut microbiota
Gao, H., Nepovimová, E., Adam, V., Heger, Z., Valko, M., Wu, Q., & Kuča, K. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1421062 · Cited by 41
“When a pathogen manages to breach the fi rst lines of defense and enters an organism, the adaptive immune system, also known as the speci fi c or acquired immune system, is triggered and begins fi ghting off the infection (185, 186).”
BackgroundVaccinology in the third millennium: scientific and social challenges
Poland, G. A., Whitaker, J. A., Poland, C. M., Ovsyannikova, I. G., & Kennedy, R. B. (2016) · Current Opinion in Virology · doi:10.1016/j.coviro.2016.03.003 · Cited by 36
Collateral Damage: Detrimental Effect of Antibiotics on the Development of Protective Immune Memory
Benoun, J. M., Labuda, J. C., & McSorley, S. J. (2016) · mBio · doi:10.1128/mbio.01520-16 · Cited by 37
Dendritic Cells in the Immune System—History, Lineages, Tissues, Tolerance, and Immunity
Austyn, J. M. (2016) · Microbiology Spectrum · doi:10.1128/microbiolspec.mchd-0046-2016 · Cited by 35
Microglia M2A Polarization as Potential Link between Food Allergy and Autism Spectrum Disorders
Kalkman, H. O., & Feuerbach, D. (2017) · Pharmaceuticals · doi:10.3390/ph10040095 · Cited by 37
“A distinctly different activation program that takes place in response to parasites, during tissue repair and in response to the cytokines IL4, IL5 and IL13 has been termed “M2” [56].”
BackgroundInfluentialA systematic approach to the development of a safe live attenuated Zika vaccine
Kwek, S. S., Watanabe, S., Chan, K. R., Ong, E. Z., Tan, H. C., Ng, W. C., Nguyen, M. T. X., Gan, E. S., Zhang, S. L.-X., Chan, K. W. K., et al. (2018) · Nature Communications · doi:10.1038/s41467-018-03337-2 · Cited by 37
Danger signals activate a putative innate immune system during regeneration in a filamentous fungus
Medina‐Castellanos, E., Villalobos‐Escobedo, J. M., Riquelme, M., Read, N. D., Abreu‐Goodger, C., & Herrera‐Estrella, A. (2018) · PLoS Genetics · doi:10.1371/journal.pgen.1007390 · Cited by 36
“Furthermore, in plants and animals, the innate immune response relies on specific proteins, the pattern-recognition receptors (PRRs), which detect conserved pathogen-associated molecular patterns and “danger” signals [2, 58].”
BackgroundPRRDB 2.0: a comprehensive database of pattern-recognition receptors and their ligands
Kaur, D., Patiyal, S., Sharma, N., Usmani, S. S., & Raghava, G. P. S. (2019) · Database · doi:10.1093/database/baz076 · Cited by 36
“Based on PRR, the innate immune system easily differentiates the type of pathogens and thus recruits the most effective form of adaptive immune response to destroy the pathogens and their toxic molecules (16–18).”
BackgroundStadtmauer, D. J., & Wagner, G. P. (2019) · Journal of Reproductive Immunology · doi:10.1016/j.jri.2019.102626 · Cited by 35
“It acts through the antigen-specific responses of the adaptive immune system, as well as pattern recognition in the form of conserved non-self structural feature recognition, and detection of loss of homeostasis (damage) or danger through functional feature recognition (Iwasaki and Medzhitov, 2015).”
BackgroundHarnessing the Complete Repertoire of Conventional Dendritic Cell Functions for Cancer Immunotherapy
Amon, L., Hatscher, L., Heger, L., Dudziak, D., & Lehmann, C. H. K. (2020) · Pharmaceutics · doi:10.3390/pharmaceutics12070663 · Cited by 37
“Within this process, the combined phenotype of signal 2 and 3 directly results from the signaling cascades downstream of environmental monitoring by DCs, thereby translating the microenvironment or select adjuvants into distinct T cell effector modules [104].”
BackgroundP2X7 receptor deletion attenuates oxidative stress and liver damage in sepsis
Larrouyet-Sarto, M. L., Tamura, A. S., Alves, V. S., Santana, P. T., Ciarlini-Magalhães, R., Rangel, T. P., Siebert, C., Hartwig, J., dos Santos, T. M., Wyse, Â. T. D. S., et al. (2020) · Purinergic Signalling · doi:10.1007/s11302-020-09746-7 · Cited by 36
Blanco-Melo, D., Nilsson-Payant, B. E., Uhl, S. A., Escudero-Pérez, B., Olschewski, S., Thibault, P. A., Panis, M., Rosenthal, M., Muñoz‐Fontela, C., Lee, B., et al. (2021) · Journal of Virology · doi:10.1128/jvi.02274-20 · Cited by 38
“IFNs signal in both autocrine and paracrine manner to induce hundreds of IFN-stimulated genes (ISGs), which collectively block many aspects of cell biology as a means to slow virus infection and provide time for the adaptive immune response to ultimately clear the pathogen (35).”
BackgroundNucleic acid and oligonucleotide delivery for activating innate immunity in cancer immunotherapy
Meng, F., Wang, J., & Yeo, Y. (2022) · Journal of Controlled Release · doi:10.1016/j.jconrel.2022.03.045 · Cited by 36
Engineered bacteria for augmented in situ tumor vaccination
Shen, X., Zhu, C., Liu, X., Zheng, H., Wu, Q., Xie, J., Huang, H., Liao, Z., Shi, J., Nan, K., et al. (2023) · Biomaterials Science · doi:10.1039/d2bm01593e · Cited by 35
Nelson, B. N., & Friedman, J. E. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25115951 · Cited by 39
“Several adaptive programs have also been described in macrophages, including priming, tolerance, and trained immunity [82,83].”
BackgroundMast cells regulate CD4+ T-cell differentiation in the absence of antigen presentation
Biefer, H. R. C., Heinbokel, T., Uehara, H., Camacho, V., Minami, K., Nian, Y., Koduru, S., Fatimy, R. E., Ghiran, I. C., Trachtenberg, A. J., et al. (2018) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2018.01.038 · Cited by 35
“Moreover, it has been reported that recognition of conserved PAMPs, such asmicrobial nucleic acids, lipoproteins, and carbohydrates, or DAMPs, which are released from injured, through intracellular or distinct PRRs expressed on DCs contribute to pathogen-specific CD4(1) T-cell responses.(12) Thus DCs and antigen prese…”
BackgroundPolumuri, S. K., Haile, L. A., Ireland, D. D. C., & Verthelyi, D. I. (2018) · Scientific Reports · doi:10.1038/s41598-018-29850-4 · Cited by 34
In vivo imaging of the immune response upon systemic RNA cancer vaccination by FDG-PET
Pektor, S., Hilscher, L., Walzer, K. C., Miederer, I., Bausbacher, N., Loquai, C., Schreckenberger, M., Şahin, U., Diken, M., & Miederer, M. (2018) · EJNMMI Research · doi:10.1186/s13550-018-0435-z · Cited by 36
Mao, R., Wu, L., Zhu, N., Liu, X., Liu, R., & Li, Y. (2019) · Nutrients · doi:10.3390/nu11040927 · Cited by 35
“Among immune cells such as dendritic cells, macrophages, NK cells, and neutrophils [22,28], macrophages and polymorphonuclear leukocytes specialize in phagocytosis, while NK cells defend against virus-infected and tumor cells.”
BackgroundHerck, S. V., & Geest, B. G. D. (2020) · Acta Pharmacologica Sinica · doi:10.1038/s41401-020-0425-3 · Cited by 36
“These include TLRs, intracellular sensors of nucleic acids such as the stimulator of interferon genes (STING) and C-type lectin receptors, among others [28].”
BackgroundInnate immune evasion by picornaviruses
Zhang, X., Paget, M., Wang, C., Zhu, Z., & Zheng, H. (2020) · European Journal of Immunology · doi:10.1002/eji.202048785 · Cited by 35
Designing the Next Generation of Vaccines: Relevance for Future Pandemics
Domínguez‐Andrés, J., van Crevel, R., Divangahi, M., & Netea, M. G. (2020) · mBio · doi:10.1128/mbio.02616-20 · Cited by 37
MicroRNAs in shaping the resolution phase of inflammation
Naqvi, R. A., Gupta, M., George, A., & Naqvi, A. R. (2021) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2021.03.019 · Cited by 35
Nanodelivery of STING agonists against cancer and infectious diseases
Zhou, J., Ventura, C. J., Fang, R. H., & Zhang, L. (2021) · Molecular Aspects of Medicine · doi:10.1016/j.mam.2021.101007 · Cited by 36
Alveolar macrophages: novel therapeutic targets for respiratory diseases
Lim, P. N., Cervantes, M. M., Pham, L. K., & Rothchild, A. C. (2021) · Expert Reviews in Molecular Medicine · doi:10.1017/erm.2021.21 · Cited by 35
Autophagy in Virus Infection: A Race between Host Immune Response and Viral Antagonism
Chawla, K., Subramanian, G., Rahman, T., Fan, S., Chakravarty, S., Gujja, S., Demchak, H., Chakravarti, R., & Chattopadhyay, S. (2022) · Immuno · doi:10.3390/immuno2010012 · Cited by 33
Meibers, H. E., Warrick, K. A., VonHandorf, A., Vallez, C. N., Kawarizadeh, K., Saha, I., Donmez, O. A., Jain, V. G., Kottyan, L. C., Weirauch, M. T., et al. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.113180 · Cited by 34
“Coordinated interactions between the innate and adaptive arms of the immune system are critical for robust and tailored immune responses 1,2 that result in elimination of the microbial threat.”
BackgroundDendritic Cells and Their Multiple Roles during Malaria Infection
Amorim, K. N. D. S., Chagas, D. C. G., Sulczewski, F. B., & Boscardin, S. B. (2016) · Journal of Immunology Research · doi:10.1155/2016/2926436 · Cited by 37
“As mentioned before, DCs express different classes of PRRs capable of recognizing PAMPs derived from a vast array of pathogens [8].”
Holmgren, A. M., McConkey, C., & Shin, S. (2016) · Cellular and Molecular Immunology · doi:10.1038/cmi.2016.36 · Cited by 35
Miao, P., Yang, D., Chen, X., Guo, Z., & Tang, Y. (2017) · Microchimica Acta · doi:10.1007/s00604-017-2419-5 · Cited by 34
“Concretely, they are essential in cell growth, migration, development and function by activating certain immune regulation pathways [3].”
BackgroundCompeting forces maintain the Hydra metaorganism
Deines, P., Lachnit, T., & Bosch, T. C. G. (2017) · Immunological Reviews · doi:10.1111/imr.12564 · Cited by 35
Vitenberga-Verza, Z., Pilmane, M., & Babjoniševa, A. (2018) · Pathology - Research and Practice · doi:10.1016/j.prp.2018.10.029 · Cited by 34
The first line of defense: effector pathways of anti-fungal innate immunity
Ward, R., & Vyas, J. M. (2020) · Current Opinion in Microbiology · doi:10.1016/j.mib.2020.10.003 · Cited by 35
Zhang, J., Zhang, Y., Xia, Y., & Sun, J. (2021) · Gut Microbes · doi:10.1080/19490976.2021.1957408 · Cited by 33
“PRRs and related pathways involved in intestinal virus sensing, such as TLRs, are mainly mediated by cell-extrinsic virus recognition.(76) We found significant alterations in PRRs, including upregulated expression of TLR3, TLR7 and NOD2 in VDR mice and increased expression of CLEC4L in VDR and VDR mice, suggesting the…”
Background'Trained immunity: consequences for lymphoid malignancies
Stevens, W. B. C., Netea, M. G., Kater, A. P., & van der Velden, W. J. F. M. (2016) · Haematologica · doi:10.3324/haematol.2016.149252 · Cited by 34
Immune escape mechanisms of severe fever with thrombocytopenia syndrome virus
Wang, T., Xu, L., Zhu, B., Wang, J., & Zheng, X. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.937684 · Cited by 33
“Antibodies produced by plasma cells can not only kill infected target cells via antibody-dependent cell-mediated cytotoxicity but also directly neutralize viruses (73).”
BackgroundRegulatory effect of sericin protein in inflammatory pathways; A comprehensive review
Rahimpour, S., Jabbari, H., Yousofi, H., Fathi, A., Mahmoodi, S., Jafarian, M. J., Shomali, N., & Shotorbani, S. S. (2023) · Pathology - Research and Practice · doi:10.1016/j.prp.2023.154369 · Cited by 33
Bauer, B. U., Knittler, M. R., Andrack, J., Berens, C., Campe, A., Christiansen, B., Fasemore, A. M., Fischer, S. F., Ganter, M., Körner, S., et al. (2023) · International Journal of Medical Microbiology · doi:10.1016/j.ijmm.2023.151590 · Cited by 35
Optimizing stem cell infusion timing in the prevention of acute graft-versus-host disease
Hou, Y., Wu, Y., Cao, Y., Hu, X., Sun, Y., Wang, H., Wang, L., Zhou, J., Zhang, Z., Liu, Z., et al. (2025) · Cell · doi:10.1016/j.cell.2025.03.022 · Cited by 35
Emerging Skin T-Cell Functions in Response to Environmental Insults
Suwanpradid, J., Holcomb, Z. E., & MacLeod, A. S. (2016) · Journal of Investigative Dermatology · doi:10.1016/j.jid.2016.08.013 · Cited by 33
“…and function of cutaneous T cells can change dramatically on environmental insults and may be driven by both antigen exposure and innate immune signals derived from surrounding keratinocytes, dendritic cells, macrophages, and other cells (Iwasaki and Medzhitov, 2015; Schroder et al., 2006).”
BackgroundJiang, G., Rocha, C. S., Hirao, L. A., Mendes, É. A., Tang, Y., Thompson, G. R., Wong, J. K., & Dandekar, S. (2017) · mBio · doi:10.1128/mbio.01518-16 · Cited by 40
“This feature is especially critical for the virus to invade and establish infection in the gut mucosa since the gastrointestinal tract is immunologically highly evolved to combat the incoming pathogens and is richly endowed with innate immune defenses (9).”
Background
Metadata
- Authors
- Iwasaki, A., & Medzhitov, R.
- Affiliations
- Howard Hughes Medical Institute (US)
- Corresponding author
- Iwasaki, Akiko
- Medzhitov, Ruslan
- Venue
- Nature Immunology
- Published
- 2015-03-19
- Volume
- 16
- Issue
- 4
- Pages
- 343-353
- ISSN
- 1529-2908 (ISSN-L)
- 1529-2916
- PMC
- PMC4507498
- OpenAlex
- W2044757050
- Cited by
- 2,160
- References
- 139
- Citations by year
- 2026: 183 · 2025: 212 · 2024: 181 · 2023: 193 · 2022: 204 · 2021: 239 · 2020: 216 · 2019: 189 · 2018: 187 · 2017: 167 · 2016: 157 · 2015: 31
- FWCI
- 17.06
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature Immunology (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- Howard Hughes Medical Institute
- National Institute of Allergy and Infectious Diseases (R01AI064705, AI062428, AI 064705, R01AI062428, AI 081884, R56AI062428, AI089771, R01AI089771, R01AI054359, R37AI046688, AI046688, R01AI081884, R01AI046688)
- National Institute of Diabetes and Digestive and Kidney Diseases (DK071754, R01DK071754)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › Immune Response and Inflammation
- Life Sciences › Immunology and Microbiology › Immunology › Immunotherapy and Immune Responses
- Life Sciences › Immunology and Microbiology › Immunology › Immune responses and vaccinations
- Keywords
- innate immunity, adaptive immunity, innate-adaptive immune crosstalk, pathogen recognition, dendritic cells, cytokines, lymphocyte activation, microbial infection, pattern recognition receptors
- MeSH terms
- Animals, Bacteria, Dendritic Cells, Fungi, Gene Expression Regulation, Helminths, Humans, Immunity, Innate, Intestines, Lung, Skin, Viruses, Lymphocyte Subsets, Cytokines, Receptors, Pattern Recognition, Adaptive Immunity
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review