Cited by 1,839Mast cells and histamineAsthma and respiratory diseasesAllergic Rhinitis and Sensitization

The DOI matches its Crossref record; 102 of the 102 references it cites were found in a registry or an index.

The development of allergic inflammation

Open access

Galli, Stephen J., Tsai, Mindy, Piliponsky, Adrian M.·2008·Nature

Open this paper in CoChat — free account

Abstract

Allergic disorders, such as anaphylaxis, hay fever, eczema and asthma, now afflict roughly 25% of people in the developed world. In allergic subjects, persistent or repetitive exposure to allergens, which typically are intrinsically innocuous substances common in the environment, results in chronic allergic inflammation. This in turn produces long-term changes in the structure of the affected organs and substantial abnormalities in their function. It is therefore important to understand the characteristics and consequences of acute and chronic allergic inflammation, and in particular to explore how mast cells can contribute to several features of this maladaptive pattern of immunological reactivity.

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

Crossref · 10.1038/nature07204

Cites

102 of 102 references verified0 citation errors · 0 not checkable

Statistics

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?

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

How regulatory T cells work
Vignali, D. A. A., Collison, L. W., & Workman, C. J. (2008) · Nature Reviews Immunology · doi:10.1038/nri2343 · Cited by 3,463
Anesthesiology
Wiklund, R. A., & Rosenbaum, S. H. (1997) · New England Journal of Medicine · doi:10.1056/nejm199710163371606 · Cited by 2,153
REGULATION OF IMMUNE RESPONSES BY TGF-β
Letterio, J. J., & Roberts, A. B. (1998) · Annual Review of Immunology · doi:10.1146/annurev.immunol.16.1.137 · Cited by 1,894
Anti-Inflammatory Cytokines
Opal, S. M., & DePalo, V. A. (2000) · Chest · doi:10.1378/chest.117.4.1162 · Cited by 1,752
The asthma epidemic
Eder, W., Ege, M. J., & von Mutius, E. (2006) · New England Journal of Medicine · doi:10.1056/nejmra054308 · Cited by 1,621
Allergy, Parasites, and the Hygiene Hypothesis
Yazdanbakhsh, M., Kremsner, P. G., & van Ree, R. (2002) · Science · doi:10.1126/science.296.5567.490 · Cited by 1,527
Immunology of asthma and chronic obstructive pulmonary disease
Barnes, P. J. (2008) · Nature reviews. Immunology · doi:10.1038/nri2254 · Cited by 1,444
New insights into atopic dermatitis
Leung, D. Y. M., Boguniewicz, M., Howell, M. D., Nomura, I., & Hamid, Q. A. (2004) · Journal of Clinical Investigation · doi:10.1172/jci21060 · Cited by 1,435
Allergy and Allergic Diseases
Kay, A. B. (2001) · New England Journal of Medicine · doi:10.1056/nejm200101043440106 · Cited by 1,368
MAST CELLS AS “TUNABLE” EFFECTOR AND IMMUNOREGULATORY CELLS: Recent Advances
Galli, S. J., Kalesnikoff, J., Grimbaldeston, M. A., Piliponsky, A. M., Williams, C. M. M., & Tsai, M. M. (2005) · Annual Review of Immunology · doi:10.1146/annurev.immunol.21.120601.141025 · Cited by 1,259
Self-citation

Show all 102 references

Research works printed but not linked: 1

von Pirquet, C. Allergie. Münch. Med. Wochenschr. 53, 1457–1458 (1906).

Sorted by citations

Items 801–900 of 1,001

Mast Cells Are Identified in the Lung Parenchyma of Wild Mice, Which Can Be Recapitulated in Naturalized Laboratory Mice
Yeh, Y., Chaudhuri, A. S., Zhou, L., Yu, F. H. Z., Boysen, P., & Xiang, Z. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.736692 · Cited by 16
Activation of succinate receptor 1 boosts human mast cell reactivity and allergic bronchoconstriction
Tang, X. Y., Rönnberg, E., Säfholm, J., Thulasingam, M., Trauelsen, M., Schwartz, T. W., Wheelock, C. E., Dahlén, S., Nilsson, G. P., & Haeggström, J. Z. (2022) · Allergy · doi:10.1111/all.15245 · Cited by 18
Immediate Hypersensitivity Reactions Induced by COVID-19 Vaccines: Current Trends, Potential Mechanisms and Prevention Strategies
Chung, W., Preclaro, I. A. C., Chung, W., & Wang, C. (2022) · Biomedicines · doi:10.3390/biomedicines10061260 · Cited by 18
Airway allergy causes alveolar macrophage death, profound alveolar disorganization and surfactant dysfunction
Feo-Lucas, L., Godio, C., de la Escalera, M. M., Ladrón, N. Á., Villarrubia, L. H., Vega‐Pérez, A., González-Cintado, L., Domínguez‐Andrés, J., García-Fojeda, B., Montero-Fernández, C., et al. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1125984 · Cited by 18
The Impact of Artificial Intelligence on Allergy Diagnosis and Treatment
Khan, M., Banerjee, S., Muskawad, S., Maity, R., Chowdhury, S. R., Ejaz, R., Kuuzie, E., & Satnarine, T. (2024) · Current Allergy and Asthma Reports · doi:10.1007/s11882-024-01152-y · Cited by 19
Polyclonal hyper-IgE mouse model reveals mechanistic insights into antibody class switch recombination
Misaghi, S., Senger, K., Sai, T., Yan, Q., Sun, Y., Hamidzadeh, K., Nguyen, A., Jin, Z., Zhou, M., Yan, D., et al. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1221661110 · Cited by 18
Inhibitory Activities of Compounds from the Marine Actinomycete Williamsia sp. MCCC 1A11233 Variant on IgE-Mediated Mast Cells and Passive Cutaneous Anaphylaxis
Gao, Y., Liu, Q., Liu, B., Xie, C., Cao, M., Yang, X., & Liu, G. (2017) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.7b04314 · Cited by 18
Inhibition of mast cell degranulation by melanin
Kawamoto, Y., Kondo, H., Hasegawa, M., Kurimoto, C., Ishii, Y., Kato, C., Botei, T., Shinya, M., Murate, T., Ueno, Y., et al. (2019) · Biochemical Pharmacology · doi:10.1016/j.bcp.2019.02.015 · Cited by 17
Inhibition of ovalbumin-induced allergic rhinitis by sumatriptan through the nitric oxide pathway in mice
Hemmati, S., Rahimi, N., Dabiri, S., Alaeddini, M., Etemad‐Moghadam, S., & Dehpour, A. R. (2019) · Life Sciences · doi:10.1016/j.lfs.2019.116901 · Cited by 18
Macmoondongtang modulates Th1-/Th2-related cytokines and alleviates asthma in a murine model
Lee, S. Y., Kang, B., Bok, S., Cho, S., & Park, D.-H. (2019) · PLoS ONE · doi:10.1371/journal.pone.0224517 · Cited by 19
Cyclic AMP in dendritic cells: A novel potential target for disease‐modifying agents in asthma and other allergic disorders
Chinn, A. M., & Insel, P. A. (2020) · British Journal of Pharmacology · doi:10.1111/bph.15095 · Cited by 18
HIF1α Deficiency in Dendritic Cells Attenuates Symptoms and Inflammatory Indicators of Allergic Rhinitis in a SIRT1-Dependent Manner
Niu, Y., Wang, J., Li, Z., Yao, K., Wang, L., & Song, J. (2020) · International Archives of Allergy and Immunology · doi:10.1159/000506862 · Cited by 18
Molecular mechanism of asthma and its novel molecular target therapeutic agent
Suraya, R., Nagano, T., Katsurada, M., Sekiya, R., Kobayashi, K., & Nishimura, Y. (2021) · Respiratory Investigation · doi:10.1016/j.resinv.2020.12.007 · Cited by 18
Molecular mechanisms and treatment modalities in equine Culicoides hypersensitivity
Fettelschoss‐Gabriel, A., Birkmann, K., Pantelyushin, S., & Kündig, T. M. (2021) · The Veterinary Journal · doi:10.1016/j.tvjl.2021.105741 · Cited by 18
Pretreatment with glycomacropeptide reduces allergen sensitization, alleviates immediate cutaneous hypersensitivity and protects from anaphylaxis
Jiménez, M., Vela, N. A. C., & Salinas, E. (2012) · Clinical & Experimental Immunology · doi:10.1111/j.1365-2249.2012.04631.x · Cited by 18
Peripheral Blood Neutrophil Activity During Dermatophagoides pteronyssinus-Induced Late-Phase Airway Inflammation in Patients with Allergic Rhinitis and Asthma
Lavinskienė, S., Jeroch, J., Malakaskas, K., Bajoriūnienė, I., Jackutė, J., & Sakalauskas, R. (2012) · Inflammation · doi:10.1007/s10753-012-9475-0 · Cited by 18
Ganoderma formosanum polysaccharides attenuate Th2 inflammation and airway hyperresponsiveness in a murine model of allergic asthma
Pi, C.-C., Wang, H.-Y., Lu, C.-Y., Lu, F. L., & Chen, C. (2014) · SpringerPlus · doi:10.1186/2193-1801-3-297 · Cited by 18
Distribution and Dynamics of Rat Basophilic Leukemia Immunoglobulin E Receptors (FcɛRI) on Planar Ligand-Presenting Surfaces
Spendier, K., Carroll‐Portillo, A., Lidke, K. A., Wilson, B. S., Timlin, J. A., & Thomas, J. L. (2010) · Biophysical Journal · doi:10.1016/j.bpj.2010.04.029 · Cited by 18
Tespa1 negatively regulates FcεRI-mediated signaling and the mast cell–mediated allergic response
Wang, D., Zheng, M., Qiu, Y., Guo, C., Ji, J., Lei, L., Zhang, X. Z., Liang, J., Lou, J. Q., Huang, W., et al. (2014) · The Journal of Experimental Medicine · doi:10.1084/jem.20140470 · Cited by 18
Bioactive Proteins and Peptides from Microalgae
Stack, J., Gouic, A. V. L., & Fitzgerald, R. J. (2020) · Wiley eBooks · doi:10.1002/9781119143802.ch61 · Cited by 18
Novel strategies for the treatment of grass pollen-induced allergic rhinitis
Larsson, O., Hellkvist, L., Peterson-Westin, U., & Cardell, L. O. (2016) · Expert Opinion on Biological Therapy · doi:10.1080/14712598.2016.1190829 · Cited by 16
Extrinsic and Intrinsic Modulators of Anaphylaxis
Carter, M. C., Park, J., Vadas, P., & Worm, M. (2023) · The Journal of Allergy and Clinical Immunology In Practice · doi:10.1016/j.jaip.2023.05.015 · Cited by 17
Biomarkers in the Clinical Development of Asthma Therapies
Staton, T. L., Choy, D. F., & Arron, J. R. (2016) · Biomarkers in Medicine · doi:10.2217/bmm.15.116 · Cited by 17
Inhibitory effect of 1,2,4,5-tetramethoxybenzene on mast cell-mediated allergic inflammation through suppression of IκB kinase complex
Je, I., Choi, H. G., Kim, H.-H., Lee, S., Choi, J. K., Kim, S., Kim, D.-S., Kwon, T. K., Shin, T., Park, P., et al. (2015) · Toxicology and Applied Pharmacology · doi:10.1016/j.taap.2015.05.006 · Cited by 17
How does allergic rhinitis impact the severity of COVID-19?: a case–control study
Güvey, A. (2021) · European Archives of Oto-Rhino-Laryngology · doi:10.1007/s00405-021-06836-z · Cited by 17
Conditioned Medium of Human Amniotic Epithelial Cells Alleviates Experimental Allergic Conjunctivitis Mainly by IL-1ra and IL-10
Wu, B., Gao, F., Lin, J., Lü, L., Xu, H., & Xu, G. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.774601 · Cited by 17
Systemic allergic contact dermatitis to palladium, platinum, and titanium: mechanisms, clinical manifestations, prevalence, and therapeutic approaches
Sadrolvaezin, A., Pezhman, A., Zare, I., Nasab, S. Z., Chamani, S., Naghizadeh, A., & Mostafavi, E. (2023) · MedComm · doi:10.1002/mco2.386 · Cited by 18
Association between allergic conditions and COVID-19 susceptibility and outcomes
Chen, C., Song, X., Murdock, D. J., Marcus, A. F., Hussein, M. A., Jalbert, J. J., & Geba, G. P. (2024) · Annals of Allergy Asthma & Immunology · doi:10.1016/j.anai.2024.01.011 · Cited by 17
A Longitudinal Study of Association between Heavy Metals and Itchy Eyes, Coughing in Chronic Cough Patients: Related with Non-Immunoglobulin E Mediated Mechanism
Nguyen, T. T. T., Higashi, T., Kambayashi, Y., Anyenda, E. O., Michigami, Y., Hara, J., Fujimura, M., Tsujiguchi, H., Kitaoka, M., Asakura, H., et al. (2016) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph13010110 · Cited by 17
Roles and relevance of mast cells in infection and vaccination
Yu, F. H. Z., & Zou, X. (2016) · Journal of Biomedical Research · doi:10.7555/jbr.30.20150038 · Cited by 17
Immunogenic peptides: B & T Cell Epitopes of Per a 10 Allergen of Periplaneta americana
Govindaraj, D., Sharma, S., Gaur, S. N. S., Lavasa, S., Prasad, N., & Arora, N. (2016) · Molecular Immunology · doi:10.1016/j.molimm.2016.10.007 · Cited by 17
LAT is essential for the mast cell stabilising effect of tHGA in IgE-mediated mast cell activation
Tan, J. W., Israf, D. A., Hashim, N. F. M., Cheah, Y. K., Harith, H. H., Shaari, K., & Tham, C. L. (2017) · Biochemical Pharmacology · doi:10.1016/j.bcp.2017.08.010 · Cited by 17
Insights into endotoxin-mediated lung inflammation and future treatment strategies
Chakraborty, A., Boer, J. C., Selomulya, C., Plebanski, M., & Royce, S. G. (2018) · Expert Review of Respiratory Medicine · doi:10.1080/17476348.2018.1523009 · Cited by 17
Organometallic Compounds and Metal Complexes in Current and Future Treatments of Inflammatory Bowel Disease and Colorectal Cancer—a Critical Review
Szczepaniak, A., & Fichna, J. (2019) · Biomolecules · doi:10.3390/biom9090398 · Cited by 17
MiR-146a Promotes Tolerogenic Properties of Dendritic Cells and through Targeting Notch1 Signaling
Tang, H., Lai, Y., Zheng, J., Chen, K., Jiang, H., & Xu, G. (2020) · Immunological Investigations · doi:10.1080/08820139.2019.1708385 · Cited by 17
Application of Polymeric Nano-Materials in Management of Inflammatory Bowel Disease
Minakshi, P., Kumar, R., Ghosh, M., Brar, B., Barnela, M., & Lakhani, P. (2020) · Current Topics in Medicinal Chemistry · doi:10.2174/1568026620666200320113322 · Cited by 17
New and old adjuvants in allergen‐specific immunotherapy: With a focus on nanoparticles
Feng, Z., Yi, X., & Hajavi, J. (2020) · Journal of Cellular Physiology · doi:10.1002/jcp.29941 · Cited by 17
Allergy is an important factor in asthma exacerbation: A Pro/Con Debate
Čustović, A., Simpson, A., Bardin, P. G., & Souëf, P. N. L. (2010) · Respirology · doi:10.1111/j.1440-1843.2010.01826.x · Cited by 17
Targeting SIRP‐α protects from type 2‐driven allergic airway inflammation
Raymond, M., Van, V. Q., Rubio, M., Welzenbach, K., & Sarfati, M. (2010) · European Journal of Immunology · doi:10.1002/eji.201040797 · Cited by 17
Effects of deuterium oxide on cell growth and vesicle speed in RBL-2H3 cells
Kalkur, R. S., Ballast, A., Triplett, A. R., & Spendier, K. (2014) · PeerJ · doi:10.7717/peerj.553 · Cited by 17
Modulatory effects of phytoglycoprotein (75 kDa) on allergic inflammatory cytokines in Di(2‐ethylhexyl) phthalate (DEHP)‐stimulated RBL‐2H3 cells
Oh, P., & Lim, K. (2009) · Journal of Cellular Biochemistry · doi:10.1002/jcb.22389 · Cited by 17
Blockade of IL-23 ameliorates allergic lung inflammation via decreasing the infiltration of Tc17 cells
Cheng, S., Chen, H., Wang, A., Bunjhoo, H., Cao, Y., Xie, J., Xu, Y., & Xiong, W. (2016) · Archives of Medical Science · doi:10.5114/aoms.2016.62923 · Cited by 17
Role of gut microbiota in idiopathic nephrotic syndrome in children
Kaneko, K., Tsuji, S., & Kimata, T. (2017) · Medical Hypotheses · doi:10.1016/j.mehy.2017.07.035 · Cited by 17
Allergic patients with and without allergen-specific immunotherapy mount protective immune responses to tick-borne encephalitis vaccination in absence of enhanced side effects or propagation of their Th2 bias
Garner‐Spitzer, E., Seidl-Friedrich, C., Zwazl, I., Hofer, M., Kinaciyan, T., Jarisch, R., Stiasny, K., Zlabinger, G. J., Kundi, M., & Wiedermann, U. (2018) · Vaccine · doi:10.1016/j.vaccine.2018.03.076 · Cited by 17
Comparative analysis of cytokine release from epithelial cell cultures of the upper airway
Shiozawa, A., Miwa, M., Ono, N., Homma, H., Hirotsu, M., & Ikeda, K. (2015) · Rhinology Journal · doi:10.4193/rhin14.078 · Cited by 17
Asthma and allergy as risk factors for suicidal behavior among young adults
Vargas, P. A., & Robles, E. (2019) · Journal of American College Health · doi:10.1080/07448481.2018.1462822 · Cited by 16
The role of regulatory T cells in the acquisition of tolerance to food allergens in children
de Quirós, E. B., Seoane-Reula, E., Alonso‐Lebrero, E., Pion, M., & Correa‐Rocha, R. (2018) · Allergologia et Immunopathologia · doi:10.1016/j.aller.2018.02.002 · Cited by 38
Therapeutic Efficacy of Flavonoids in Allergies: A Systematic Review of Randomized Controlled Trials
Brasiel, P. G. D. A., Guimarães, F. V., Rodrigues, P. M., Bou‐Habib, D. C., & Carvalho, V. F. (2022) · Journal of Immunology Research · doi:10.1155/2022/8191253 · Cited by 19
Bisdemethoxycurcumin attenuates OVA‑induced food allergy by inhibiting the MAPK and NF‑κB signaling pathways
Wang, Y., Zhang, P., Zhang, J., & Hong, T. (2022) · Experimental and Therapeutic Medicine · doi:10.3892/etm.2022.11328 · Cited by 16
Treating allergies via skin – Recent advances in cutaneous allergen immunotherapy
Nesovic, L. D., Shakya, A. K., & Gill, H. S. (2022) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2022.114458 · Cited by 17
Treatment of allergy: Overview of synthetic anti-allergy small molecules in medicinal chemistry
Zhang, S., Liu, Y., Javeed, A., Jian, C., Sun, J., Wu, S., & Han, B. (2023) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2023.115151 · Cited by 16
Structures and Anti-Allergic Activities of Natural Products from Marine Organisms
Chen, N., Zhang, S., Javeed, A., Jian, C., Liu, Y., Sun, J., Wu, S., Fu, P., & Han, B. (2023) · Marine Drugs · doi:10.3390/md21030152 · Cited by 16
Aberrant expression of suppressor of cytokine signaling ( SOCS ) molecules contributes to the development of allergic diseases
Jafarzadeh, A., Chauhan, P. S., Nemati, M., Jafarzadeh, S., & Yoshimura, A. (2023) · Clinical & Experimental Allergy · doi:10.1111/cea.14385 · Cited by 16
Eosinophils Interaction with Mast Cells: The Allergic Effector Unit
Gangwar, R. S., & Levi‐Schaffer, F. (2014) · Methods in molecular biology · doi:10.1007/978-1-4939-1016-8_20 · Cited by 16
Glycomacropeptide: Biological Activities and Uses
Jáuregui-Rincón, J., Miralles, E. M. S., Vela, N. A. C., & Jiménez, M. (2019) · IntechOpen eBooks · doi:10.5772/intechopen.82144 · Cited by 16
MiR-202-5p/MATN2 are associated with regulatory T-cells differentiation and function in allergic rhinitis
Wang, L., Yang, X., Li, W., Song, X., & Kang, S. (2019) · Human Cell · doi:10.1007/s13577-019-00266-0 · Cited by 16
Raw Milk-Induced Protection against Food Allergic Symptoms in Mice Is Accompanied by Shifts in Microbial Community Structure
Abbring, S., Engen, P. A., Naqib, A. D., Green, S. J., Garssen, J., Keshavarzian, A., & van Esch, B. C. A. M. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22073417 · Cited by 16
A multi‐disciplinary approach to the diagnosis and management of allergic diseases: An EAACI Task Force
Vassilopoulou, Ε., Skypala, I. J., Feketea, G. M., Gawlik, R., DunnGalvin, A., Meyer, R. W., Pitsios, C., Pop, R. M., Ryan, D. P., Said, M., et al. (2021) · Pediatric Allergy and Immunology · doi:10.1111/pai.13692 · Cited by 16
Harnessing the Anti-Tumor Mediators in Mast Cells as a New Strategy for Adoptive Cell Transfer for Cancer
Fereydouni, M., Motaghed, M., Ahani, E., Kafri, T., Dellinger, K., Metcalfe, D. D., & Kepley, C. L. (2022) · Frontiers in Oncology · doi:10.3389/fonc.2022.830199 · Cited by 16
Novel binuclear μ-oxo diruthenium complexes combined with ibuprofen and ketoprofen: Interaction with relevant target biomolecules and anti-allergic potential
Seuanes, G. C., Moreira, M. B., Petta, T., Lama, M. P. F. D. M. D., de Moraes, L. A. B., de Oliveira, A. R. M., Naal, R. M. Z. G., & Nikolaou, S. (2015) · Journal of Inorganic Biochemistry · doi:10.1016/j.jinorgbio.2015.08.004 · Cited by 16
I g E knock‐in mice suggest a role for high levels of I g E in basophil‐mediated active systemic anaphylaxis
Lübben, W., Turqueti‐Neves, A., Okhrimenko, A., Stöberl, C., Schmidt, V., Pfeffer, K., Dehnert, S., Wünsche, S., Storsberg, S., Paul, S., et al. (2013) · European Journal of Immunology · doi:10.1002/eji.201242675 · Cited by 16
Risk of idiopathic nephrotic syndrome among children with asthma: a nationwide, population-based cohort study
Wei, C., Lin, C., Shen, T., & Li, Y. (2015) · Pediatric Research · doi:10.1038/pr.2015.80 · Cited by 16
The Immunomodulatory Effect of You-Gui-Wan onDermatogoides-pteronyssinus-Induced Asthma
Lin, L., Lin, C.-C., Wang, S.-D., Chao, Y., & Kao, S.-T. (2012) · Evidence-based Complementary and Alternative Medicine · doi:10.1155/2012/476060 · Cited by 16
The emerging role of interleukin-21 in allergic diseases (Review)
Gong, F., SU, Q., PAN, Y. H., Huang, X., & SHEN, W. H. (2013) · Biomedical Reports · doi:10.3892/br.2013.166 · Cited by 16
Sinonasal Epithelial Cell Response toStaphylococcus aureusBurden in Chronic Rhinosinusitis
Kohanski, M. A., & Lane, A. P. (2015) · JAMA Otolaryngology–Head & Neck Surgery · doi:10.1001/jamaoto.2014.3550 · Cited by 16
Crowdsourcing without Data Bias: Building a Quality Assurance System for Air Pollution Symptom Mapping
Samulowska, M., Chmielewski, S., Raczko, E., Lupa, M., Myszkowska, D., & Zagajewski, B. (2021) · ISPRS International Journal of Geo-Information · doi:10.3390/ijgi10020046 · Cited by 16
The Targets of IgE: Allergen-Associated and Tumor-Associated Molecular Patterns
Jensen‐Jarolim, E., Mechtcheriakova, D., & Pali‐Schöll, I. (2009) · Humana Press eBooks · doi:10.1007/978-1-60761-451-7_10 · Cited by 16
Individualized treatment for allergic rhinitis based on key nasal clinical manifestations combined with histamine and leukotriene D4 levels
Shen, C., Chen, F., Wang, H., Zhang, X., Li, G., & Wen, Z. (2018) · Brazilian Journal of Otorhinolaryngology · doi:10.1016/j.bjorl.2018.09.007 · Cited by 15
Drug repurposing: Clemastine fumarate and neurodegeneration
Zhu, J., Ma, R., & Li, G. (2022) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2022.113904 · Cited by 16
Bronchiectasis in severe asthma is associated with eosinophilic airway inflammation and activation
Frøssing, L., von Bülow, A., & Porsbjerg, C. M. (2022) · Journal of Allergy and Clinical Immunology Global · doi:10.1016/j.jacig.2022.10.001 · Cited by 15
Targeting the Semaphorin3E-plexinD1 complex in allergic asthma
Matloubi, M., Koussih, L., Shan, L., Lukawy, C., & GOUNNI, A. S. (2022) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2023.108351 · Cited by 14
Mast cells contribute to the resolution of allergic inflammation by releasing resolvin D1
Puzzovio, P. G., Pahima, H. T., George, T., Mankuta, D., Eliashar, R., Tiligada, E., Levy, B. D., & Levi‐Schaffer, F. (2023) · Pharmacological Research · doi:10.1016/j.phrs.2023.106691 · Cited by 15
Modulation of the Immune Response to Allergies Using Alternative Functional Foods
López-Enríquez, S., Múnera‐Rodríguez, A. M., Leiva‐Castro, C., Sobrino, F., & Palomares, F. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms25010467 · Cited by 15
The Role of Extracellular Vesicles in Atopic Dermatitis
Harvey-Seutcheu, C., Hopkins, G. V., & Fairclough, L. C. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25063255 · Cited by 17
The critical roles of IGFs in immune modulation and inflammation
Wang, X., Cao, L., Liu, S., Zhou, Y., Zhou, J., Zhao, W., Gao, S., Liu, R., Shi, Y., Shao, C., et al. (2024) · Cytokine · doi:10.1016/j.cyto.2024.156750 · Cited by 17
Risk of bipolar disorder among adolescents with allergic rhinitis: A nationwide longitudinal study
Chen, M., Lan, W.-H., Hsu, J.-W., Huang, K., Chen, Y.-S., Li, C., Lin, W.-C., Chang, W.-H., Chen, T., Pan, T., et al. (2015) · Journal of Psychosomatic Research · doi:10.1016/j.jpsychores.2015.08.009 · Cited by 16
Insulin Modulates Cytokine Release, Collagen and Mucus Secretion in Lung Remodeling of Allergic Diabetic Mice
Ferreira, S. S. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.00633 · Cited by 15
Study of the allergenic potential of Bacillus thuringiensis Cry1Ac toxin following intra-gastric administration in a murine model of food-allergy
Santos-Vigil, K. I., Ilhuicatzi-Alvarado, D., García‐Hernández, A. L., Herrera-García, J. S., & Moreno‐Fierros, L. (2018) · International Immunopharmacology · doi:10.1016/j.intimp.2018.05.029 · Cited by 15
Update on Eosinophil Interaction with Mast Cells: The Allergic Effector Unit
Gangwar, R. S., Pahima, H. T., Puzzovio, P. G., & Levi‐Schaffer, F. (2021) · Methods in molecular biology · doi:10.1007/978-1-0716-1095-4_18 · Cited by 15
IL-33 priming amplifies ATP-mediated mast cell cytokine production
Straus, D. B., Pryor, D. T., Haque, T. T., Kee, S. A., Dailey, J. M., Jackson, K. G., Barnstein, B. O., & Ryan, J. J. (2021) · Cellular Immunology · doi:10.1016/j.cellimm.2021.104470 · Cited by 15
The Lung
Husain, A. N. (2010) · Elsevier eBooks · doi:10.1016/b978-1-4377-0792-2.50020-1 · Cited by 15
Suppression of mast-cell-mediated allergic inflammation by Lindera obtusiloba
Suh, W. M., Park, S.-B., Lee, S., Kim, H.-H., Suk, K., Son, J., Kwon, T. K., Choi, H. G., Lee, S., & Kim, S. (2011) · Experimental Biology and Medicine · doi:10.1258/ebm.2010.010274 · Cited by 15
Immunomodulatory Effects of Escherichia coli ATCC 25922 on Allergic Airway Inflammation in a Mouse Model
Pang, W., Wang, H., Shi, L., Sun, Y., Wang, X., Wang, M., Li, J., Wang, H., & Shi, G. (2013) · PLoS ONE · doi:10.1371/journal.pone.0059174 · Cited by 14
Vigna angularis inhibits mast cell-mediated allergic inflammation
Kim, H.-H., Kim, S. W., KIM, D.-S., Oh, H., Rho, M., & Kim, S. (2013) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2013.1430 · Cited by 15
Aqueous Extract ofMosla chinensisInhibits Mast Cell-Mediated Allergic Inflammation
Kim, H.-H., Yoo, J.-S., Shin, T., & Kim, S. (2012) · The American Journal of Chinese Medicine · doi:10.1142/s0192415x12500930 · Cited by 15
Anti-allergic potential of Typhonium blumei: Inhibition of degranulation via suppression of PI3K/PLCγ2 phosphorylation and calcium influx
Kořínek, M., Chen, K., Jiang, Y.-H., El‐Shazly, M., Stocker, J., Chou, C., Hwang, T., Wu, Y., Chen, B., & Chang, F. (2016) · Phytomedicine · doi:10.1016/j.phymed.2016.10.011 · Cited by 16
Allium�hookeri root extract regulates asthmatic changes through immunological modulation of Th1/Th2‑related factors in an ovalbumin‑induced asthma mouse model
Bok, S., Seo, J., Bae, C., Kang, B., Cho, S., & Park, D. (2019) · Molecular Medicine Reports · doi:10.3892/mmr.2019.10560 · Cited by 15
Natural products targeting FcεRI receptor for anti‐allergic therapeutics
Vo, T. S. (2020) · Journal of Food Biochemistry · doi:10.1111/jfbc.13335 · Cited by 15
Effects of Hyeonggaeyeongyo-Tang in Ovalbumin-Induced Allergic Rhinitis Model
Hong, S. H., Kim, S. R., Choi, H., Ku, J. M., Seo, H. S., Shin, Y. C., & Ko, S. (2014) · Mediators of Inflammation · doi:10.1155/2014/418705 · Cited by 15
Comparative Microarray Analysis and Pulmonary Changes in Brown Norway Rats Exposed to Ovalbumin and Concentrated Air Particulates
Heidenfelder, B. L., Reif, D. M., Harkema, J. R., Hubal, E. A. C., Hudgens, E., Bramble, L. A., Wagner, J. G., Morishita, M., Keeler, G. J., Edwards, S. W., et al. (2009) · Toxicological Sciences · doi:10.1093/toxsci/kfp005 · Cited by 15
[Livedo reticularis and cerebrovascular accidents].
Beurey, J., Weber, M., Edelson, F., Thomas, I., & Eich, D. (1984) · PubMed · Cited by 15
Structural and Functional Insights Into IgE Receptor Interactions and Disruptive Inhibition
Eggel, A., & Jardetzky, T. S. (2025) · Immunological Reviews · doi:10.1111/imr.70031 · Cited by 14
Multimorbidity and Serological Response to SARS-CoV-2 Nine Months after 1st Vaccine Dose: European Cohort of Healthcare Workers—Orchestra Project
Violán, C., Carrasco-Ribelles, L. A., Collatuzzo, G., Ditano, G., Abedini, M., Janke, C., Reinkemeyer, C., Thi, T. G. L., Liviero, F., Scapellato, M. L., et al. (2023) · Vaccines · doi:10.3390/vaccines11081340 · Cited by 14
S. aureus biofilm metabolic activity correlates positively with patients’ eosinophil frequencies and disease severity in chronic rhinosinusitis
Shaghayegh, G., Cooksley, C. M., Bouras, G. S., Houtak, G., Nepal, R., Psaltis, A. J., Wormald, P., & Vreugde, S. (2023) · Microbes and Infection · doi:10.1016/j.micinf.2023.105213 · Cited by 14
Vernal Keratoconjunctivitis: Immunopathological Insights and Therapeutic Applications of Immunomodulators
Hehar, N. K., & Chigbu, D. I. (2024) · Life · doi:10.3390/life14030361 · Cited by 14
Is Nasal Dysbiosis a Required Component for Neuroinflammation in Major Depressive Disorder?
Vásquez-Pérez, J. M., González‐Guevara, E., Gutiérrez-Buenabad, D., Martínez‐Gopar, P. E., Martínez‐Lazcano, J. C., & Cárdenas, G. (2024) · Molecular Neurobiology · doi:10.1007/s12035-024-04375-2 · Cited by 16
Cheonggukjang Ethanol Extracts Inhibit a Murine Allergic Asthma via Suppression of Mast Cell-Dependent Anaphylactic Reactions
Bae, M., Shin, H. S., See, H.-J., Chai, O. H., & Shon, D. (2014) · Journal of Medicinal Food · doi:10.1089/jmf.2013.2997 · Cited by 14
Topical Application of Fingolimod Perturbs Cutaneous Inflammation
Sun, W. Y., Dimasi, D. P., Pitman, M. R., Zhuang, Y., Heddle, R. J., Pitson, S. M., Grimbaldeston, M. A., & Bonder, C. S. (2016) · The Journal of Immunology · doi:10.4049/jimmunol.1501510 · Cited by 14
Age-Related Changes in Immunological Factors and Their Relevance in Allergic Disease Development During Childhood
Chang, W., Kim, E., Lim, Y., Yoon, D., Son, J.-Y., Park, J., Hong, S., Cho, S., & Lee, J.-S. (2016) · Allergy Asthma and Immunology Research · doi:10.4168/aair.2016.8.4.338 · Cited by 15
Silkworm dropping extract regulates food allergy symptoms via inhibition of Th2‐related responses in an ovalbumin‐induced food allergy model
Jung, S. Y., See, H., Kwon, D., Choi, D., Lee, S., Shon, D., & Shin, H. S. (2019) · Journal of the Science of Food and Agriculture · doi:10.1002/jsfa.9993 · Cited by 16

Authors: Galli, S. J., Tsai, M., & Piliponsky, A. M.
Affiliations: Stanford Medicine (US)
ORCID: Galli, Stephen J.
Tsai, Mindy
Piliponsky, Adrian M.
Venue: Nature
Publisher: Springer Science and Business Media LLC
Published: 2008-07-01
Volume: 454
Issue: 7203
Pages: 445-454
ISSN: 0028-0836 (ISSN-L)
1476-4687
DOI: 10.1038/nature07204
PMC: PMC3573758
OpenAlex: W2007589345
Cited by: 1,839
References: 102
Citations by year: 2026: 75 · 2025: 80 · 2024: 100 · 2023: 127 · 2022: 117 · 2021: 113 · 2020: 133 · 2019: 125 · 2018: 97 · 2017: 101 · 2016: 102 · 2015: 94 · 2014: 124 · 2013: 106 · 2012: 95
FWCI: 6.11
Type: journal article
Language: en
Open access: green
www.ncbi.nlm.nih.gov
Licence: www.springer.com/tdm (tdm)
www.springer.com/tdm (vor)
Locations: Nature (publishedVersion)
PubMed (publishedVersion)
Europe PMC (PubMed Central) (acceptedVersion)
PubMed Central (acceptedVersion)
RePEc: Research Papers in Economics (submittedVersion)
Funders: National Institutes of Health
National Cancer Institute (R01CA072074)
National Institute of Allergy and Infectious Diseases (R01AI023990, R01AI070813)
Topics: Life Sciences › Immunology and Microbiology › Immunology › Mast cells and histamine
Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Asthma and respiratory diseases
Health Sciences › Medicine › Immunology and Allergy › Allergic Rhinitis and Sensitization
Keywords: allergic inflammation, mast cells, anaphylaxis, allergic rhinitis, atopic dermatitis, asthma, allergen exposure, chronic inflammation, hypersensitivity
MeSH terms: Allergens, Animals, Chronic Disease, Epithelium, Humans, Hypersensitivity, Immunoglobulin E, Inflammation

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

The development of allergic inflammation

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Claims other papers make about this one

Self-check

Citations

Cites

Cited by

Related

Metadata

Record

About these checks