Towards an understanding of the adjuvant action of aluminium

Two types of murine helper T cell clone. I. Definition according to profiles of lymphokine activities and secreted proteins.

Mosmann, T. R., Cherwinski, H. M., Bond, M. W., Giedlin, M. A., & Coffman, R. L. (1986) · The Journal of Immunology · doi:10.4049/jimmunol.136.7.2348 · Cited by 7,553

Gout-associated uric acid crystals activate the NALP3 inflammasome

Martinon, F., Pétrilli, V., Mayor, A., Tardivel, A., & Tschopp, J. (2006) · Nature · doi:10.1038/nature04516 · Cited by 5,326

Silica crystals and aluminum salts activate the NALP3 inflammasome through phagosomal destabilization

Hornung, V., Bauernfeind, F., Halle, A., Samstad, E. O., Kono, H., Rock, K. L., Fitzgerald, K. A., & Latz, E. (2008) · Nature Immunology · doi:10.1038/ni.1631 · Cited by 3,065

Innate Immune Activation Through Nalp3 Inflammasome Sensing of Asbestos and Silica

Dostert, C., Pétrilli, V., Van Bruggen, R., Steele, C., Mossman, B. T., & Tschopp, J. (2008) · Science · doi:10.1126/science.1156995 · Cited by 2,658 · cited 1×

How dying cells alert the immune system to danger

Kono, H., & Rock, K. L. (2008) · Nature Reviews Immunology · doi:10.1038/nri2215 · Cited by 1,737

Molecular identification of a danger signal that alerts the immune system to dying cells

Shi, Y., Evans, J. E., & Rock, K. L. (2003) · Nature · doi:10.1038/nature01991 · Cited by 1,684

Crucial role for the Nalp3 inflammasome in the immunostimulatory properties of aluminium adjuvants

Eisenbarth, S. C., Colegio, O. R., O’Connor, W., Sutterwala, F. S., & Flavell, R. A. (2008) · Nature · doi:10.1038/nature06939 · Cited by 1,542

Toll-like receptors control activation of adaptive immune responses

Schnare, M., Barton, G. M., Czopik, A. K., Takeda, K., Akira, S., & Medzhitov, R. M. (2001) · Nature Immunology · doi:10.1038/ni712 · Cited by 1,364

Disruption of the murine IL-4 gene blocks Th2 cytokine responses

Köpf, M., Gros, G. S. L., Bachmann, M. F., Lamers, M. C., Bluethmann, H., & Köhler, G. (1993) · Nature · doi:10.1038/362245a0 · Cited by 1,202

Alum adjuvant boosts adaptive immunity by inducing uric acid and activating inflammatory dendritic cells

Kool, M., Soullié, T., van Nimwegen, M., Willart, M. A. M., Muskens, F., Jung, S., Hoogsteden, H. C., Hammad, H., & Lambrecht, B. N. (2008) · The Journal of Experimental Medicine · doi:10.1084/jem.20071087 · Cited by 1,014

Correction of age-associated defects in dendritic cell functions enables CD4 + T cells to eradicate tumors in the elderlyPreprint

Zhivaki, D., Borriello, F., Kennedy, S. N., Evavold, C. L., Bahleda, K. M., Chapman, K. L., Zanoni, I., & Kagan, J. C. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.11.08.515695 · Cited by 2

Al-fumarate, a Metal-Organic Framework encapsulating antigen as a potent, versatile and resorbable vaccine adjuvantPreprint

Christodoulou, I., Gkaniatsou, E., Bourdreux, F., Haouas, M., Steunou, N., Patriarche, G., Djédiat, C., Pagnon-Minot, A., Lecerf, C., Lopez, M., et al. (2023) · ChemRxiv · doi:10.26434/chemrxiv-2023-hhw0t · Cited by 1

Enhancing protective efficacy and immunogenicity of hemagglutinin-based influenza vaccine utilizing adjuvants developed by BECCPreprint

Das, S., Tenaglia, B. M., Riley, D., Speed, S., Baracco, L., Gardner, F. M., Varisco, D. J., Yang, H., Nijhuis, H., Kerstetter, L. J., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.06.03.657703 · Cited by 2

Vaccines

Perrie, Y., Kaur, R., & Henriksen‐Lacey, M. (2013) · Springer eBooks · doi:10.1007/978-1-4614-9164-4_17 · Cited by 1

Overview of the immune system and introduction to vaccines

Hillery, A. M. (2024) · Elsevier eBooks · doi:10.1016/b978-0-443-28934-7.00002-9 · Cited by 1

Enhanced Antitumor Immunity of a Globo H‐Based Vaccine Enabled by the Combination Adjuvants of 3D‐MPL and QS‐21

Ma, W., Xu, Z., Teng, C., Cao, C., Wu, R., Meng, X., Sui, Q., Gao, Q., Zong, C., & Li, T. (2024) · Angewandte Chemie · doi:10.1002/ange.202418948 · Cited by 1

Photoconverted cells allow rapid assessment of vaccine adjuvant potency in mice

Zhong, Y., Chen, M., Lin, H., Zu, C., He, Y., & Wang, B. (2025) · iScience · doi:10.1016/j.isci.2025.112774 · Cited by 1

Immunomodulatory activities of carbon quantum dots on the primary macrophages and whole splenocytes

Ayaz, F., Kavrak, B., Bilakaya, B., Çamlık, G., Özarslan, F., & Değim, İ. T. (2025) · Immunologic Research · doi:10.1007/s12026-025-09652-3 · Cited by 1

Induction of Sustained Immunity Following Vaccination with Live Attenuated Trypanosoma cruzi Parasites Combined with Saponin-Based Adjuvants

Zabala, B. A., Vázquez, M. E., Barraza, D. E., Mesías, A. C., Ramos, F., Uncos, A. D., Marcipar, I. S., Acuña, L., & Brandán, C. P. (2025) · Biology · doi:10.3390/biology14091298 · Cited by 1

Introduction to the Immune System

McComb, S., Thiriot, A., Akache, B., Krishnan, L., & Stark, F. C. (2025) · Methods in molecular biology · doi:10.1007/978-1-0716-4832-2_1 · Cited by 1

Survivin targeting triple-fusion vaccine DCSurvivin-LTB inhibits tumor growth in mouse model of triple-negative breast cancer

Rashid, A., Krishnan, A., Gupta, S., Gupta, J. C., & Talwar, G. P. (2025) · Medical Oncology · doi:10.1007/s12032-025-03152-y · Cited by 1

Immune Responses and Protective Efficacy of Nanoemulsion-Adjuvanted Monkeypox Virus Recombinant Vaccines Against Lethal Challenge in Mice

Zhang, C., Liu, N., Zhao, Y., Pan, Z., Wang, D., Tang, W., He, Y., Xu, Z., Qi, Z., Zhang, X., et al. (2025) · Pathogens · doi:10.3390/pathogens14121293 · Cited by 1

Nanoparticle Vaccines Based on the Truncated VZV gE Elicit a Robust Immune Response in Mice

Shi, T., Hai, L., Wu, J., Hu, H., Jiang, J., Wang, R., Li, Z., Cui, Q., Fu, S., Nie, K., et al. (2026) · Vaccines · doi:10.3390/vaccines14010069 · Cited by 1

Immunogenicity and protection mediated by dmLT and alum adjuvants for an HIV-1 vaccine

Stokdyk, K., Sahoo, A., Gangadhara, S., Williams, L. D., Styles, T. M., Hellman, C. A., Zhang, L., Odeh, A. J., Flaherty, S., Shen, X., et al. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1706958 · Cited by 1

A protein-based pneumococcal vaccine elicits broad immunity associated with multifunctional antibody responses in humans

Li, K., Yang, J., Zhai, X., Gou, J.-B., Sui, X., Wei, B., Wang, Y., Su, X., Yang, X., Jin, S., et al. (2026) · Journal of Clinical Investigation · doi:10.1172/jci196261 · Cited by 2

Heterologous saRNA prime – multivalent protein boost strategy induces broad and durable immunity against SARS-CoV-2 and MERS-CoV

Renn, D., McPartlan, J. S., Banala, S., Kiessling, F. M., Talukder, P., Mandl, C. W., Eppinger, J., Chahal, J. S., & Rueping, M. (2026) · Scientific Reports · doi:10.1038/s41598-026-44645-8 · Cited by 1

Recent Advances, Bottlenecks, and Future Directions in Plasmodium falciparum Vaccine Development

Turan, G., Boggio, M. J., Othman, A. S., Nnaemeka, V., Hill, A. V. S., & Salman, A. M. (2026) · Vaccines · doi:10.3390/vaccines14030277 · Cited by 2

Leishmania Extracellular Vesicles as a Preventive Vaccine Platform Against Leishmaniasis

Yilmaz, I. C., Tokmak, I., Yıldırım, M., Yildirim, T. C., Ozkoc, E. S., Evcili, İ., İpekoğlu, E. M., Ayanoğlu, İ. C., Dunuroglu, E., Caliskan, D., et al. (2026) · Journal of Extracellular Vesicles · doi:10.1002/jev2.70252 · Cited by 1

Polygonatum sibiricum Polysaccharide and αGalCer Synergistically Act as Dual Adjuvants to Enhance Humoral and Cellular Immune Responses

Liu, J., Wang, J., He, Y., Huang, Y., Quan, W., Mu, H., Gou, J., & Peng, X. (2026) · Molecular Pharmaceutics · doi:10.1021/acs.molpharmaceut.6c00283 · Cited by 1

DAMPs and adjuvant

Kojima, M., Ori, D., & Kawai, T. (2026) · Current Opinion in Virology · doi:10.1016/j.coviro.2026.101531 · Cited by 1

Personalized Biomineralized Tumor Whole-Component Vaccine for Synergistic cGAS-STING/aTIGIT Immunotherapy

Zhang, X., Shi, Y., Xie, S., Yi, Z., Jiang, Z., Wang, Y., & Zha, Z. (2026) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.6c04668 · Cited by 1

Adjuvants orchestrate cross-organ induction of mucosal CD8+ T cell immune responses in respiratory tracts

Jiang, J., Hong, J., Yang, H., Yang, H., Chen, Y., Wei, Y., Deng, C., Peng, L., & Wang, J. (2026) · The Journal of Immunology · doi:10.1093/jimmun/vkag117 · Cited by 1

The discovery and development of small molecule immune potentiators (SMIPs) as next-generation vaccine adjuvants, the creation of AS37

Ianni, E., Stranges, D., & O’Hagan, D. T. (2026) · Current Opinion in Virology · doi:10.1016/j.coviro.2026.101568 · Cited by 1

Development of a broadly reactive vaccine for highly pathogenic H5N1 influenza

Giles, B. M. (2011) · D-Scholarship@Pitt (University of Pittsburgh) · Cited by 1

Liposomes and Other Nanoparticles as Cancer Vaccines and Immunotherapeutics

Altin, J. G. (2012) · Springer eBooks · doi:10.1007/978-94-007-4543-8_7 · Cited by 1

Vaccine and Immunotherapy Delivery

Irvine, D. J., & Jewell, C. M. (2011) · Elsevier eBooks · doi:10.1016/b978-0-08-055294-1.00132-x · Cited by 1

Beneficial effects of the mixed adjuvant of CpG plus monophosphoryl lipid a in immunization with a recombinant protein vaccine for hepatitis A

Hwang, I., Choi, D., See, H.-J., Kim, W., Chung, I. S., & Shon, D. (2013) · Journal of the Korean Society for Applied Biological Chemistry · doi:10.1007/s13765-012-2398-5 · Cited by 1

Nasal vaccination using novel mucosal adjuvants : with main focus on influenza A virus

Falkeborn, T. (2015) · Linköping University Electronic Press eBooks · doi:10.3384/diss.diva-117981 · Cited by 1

A critical appraisal of Ixiaro® – a cell-derived inactivated vaccine for Japanese encephalitis

Jones, D. (2009) · Virus Adaptation and Treatment · doi:10.2147/vaat.s6105 · Cited by 1

Stimulation of dendritic cells with vaccine and vaccine–antibody complex and effect on immune response

HATİPOGLU, I. H., Söğüt, İ., Ercan, D., Aksu, S., Sivas, H., & Başalp, A. (2013) · TURKISH JOURNAL OF BIOLOGY · doi:10.3906/biy-1209-36 · Cited by 1

Nanostructures for Oral Vaccine Delivery

Gamazo, C., & Irache, J. M. (2012) · Royal Society of Chemistry eBooks · doi:10.1039/9781849735292-00091 · Cited by 1

Development of an oral immunoadjuvant from cheonggukjang that is efficacious for both mucosal and systemic immunity

Hwang, I., Choi, D., See, H.-J., Lim, S., Kim, W., Chung, I. S., & Shon, D. (2013) · Food Science and Biotechnology · doi:10.1007/s10068-014-0033-4 · Cited by 1

Uricase Inhibits Nitrogen Dioxide–Promoted Allergic Sensitization to Inhaled Ovalbumin Independent of Uric Acid Catabolism

Ather, J. L., Burgess, E. J., Hoyt, L. R., Randall, M. J., Mandal, M. K., Matthews, D. E., Boyson, J. E., & Poynter, M. E. (2016) · The Journal of Immunology · doi:10.4049/jimmunol.1600336 · Cited by 1

Particulate-Driven Type-2 Immunity and Allergic Responses

Kuroda, E., Temizoz, B., Coban, C., Ozasa, K., & Ishii, K. J. (2016) · Current topics in environmental health and preventive medicine · doi:10.1007/978-981-10-0351-6_5 · Cited by 1

Optimization and analisys of vaccination schedules using simulated annealing and agent based models

Pennisi, M. A., Russo, G. L., Sanchez-Lantaron, J. A., Reche, P. A., & Pappalardo, F. (2017) · IEEE International Conference on Bioinformatics and Biomedicine (BIBM) · doi:10.1109/bibm.2017.8217877 · Cited by 1

Glycomic studies of parasitic nematodes

Sutov, G. (2015) · doi:10.25560/56060 · Cited by 1

Results of Pre-Clinical and Clinical Tests of Organic Hydroxyapatite as Adjuvant of Bacterial Vaccine

Agoltsov, V. A., Popova, O. M., Veselovsky, S. Y., Частов, А. А., Semivolos, A. M., & Solotova, N. V. (2019) · Advances in Animal and Veterinary Sciences · doi:10.17582/journal.aavs/2019/7.7.583.592 · Cited by 1

Applications of biosurfactants as nonpyrogenic and nontoxic immunologic adjuvants

Pervaiz, W., Akash, M. S. H., Victor, F., & Rehman, K. (2022) · Elsevier eBooks · doi:10.1016/b978-0-323-85146-6.00021-8 · Cited by 1

Sex-differential non-specific effects of adjuvanted and non-adjuvanted rabies vaccines versus placebo on all-cause mortality in dogs (NERVE-Dog study): a study protocol for a randomized controlled trial with a nested case–control study

Knobel, D. L., Conan, A., Toka, F. N., Arega, S. M., Byaruhanga, C., Ogola, E., Muok, E. M. O., Crafford, J. E., Leisewitz, A. L., Quan, M., et al. (2022) · BMC Veterinary Research · doi:10.1186/s12917-022-03455-6 · Cited by 1

Vaccine adjuvants and carriers

Sarthak, S., Pasupuleti, D., Emmanuel, A., Bansal, A., Joshi, D., Patil, S., Bagwe, P., Uddin, M. N., & D’Souza, M. J. (2024) · Elsevier eBooks · doi:10.1016/b978-0-443-18564-9.00022-9 · Cited by 1

Systems Biology: A New Era for Vaccine Development; from Deductive Toward Inductive

Debnath, U., & Ghosh, S. (2024) · Springer eBooks · doi:10.1007/978-981-99-9462-5_13 · Cited by 1

Adjuvanted Modified Bacterial Antigens for Single-Dose Vaccines

Benedetto, R. D., Massai, L., Wright, M., Mancini, F., Cleveland, M., Rossi, O., Giannelli, C., Scorza, F. B., & Micoli, F. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms252111461 · Cited by 1

Elucidating the porous structure of aluminum adjuvants via in-situ small-angle scattering technique

Rinee, K. C., Patton, Z. E., Gillilan, R. E., Huang, Q., Pingali, S. V., Heroux, L., & Xu, A. Y. (2025) · Vaccine · doi:10.1016/j.vaccine.2025.126813 · Cited by 1

Non-conjugated TLR agonists increase the quantity of antibodies but not their quality in a murine immunization model

Aymerich, N., Bucheli, O. T. M., Portmann, K., Schlotheuber, L. J., Sigvaldadóttir, I., Baudry, J., & Eyer, K. (2025) · Vaccine · doi:10.1016/j.vaccine.2025.127518 · Cited by 2

Metal Oxides and Related Nanostructures

Zhou, R. (2015) · Springer eBooks · doi:10.1007/978-3-319-15382-7_7 · Cited by 1

Interactions Between Antigens and Nanoemulsion Adjuvants: Separation and Characterization Techniques

Chan, M. Y., Fedor, D. M., Phan, T., Barnes, L., V, & Kramer, R. M. (2016) · Methods in molecular biology · doi:10.1007/978-1-4939-6445-1_21 · Cited by 1

Supercritical Carbon Dioxide Extract of Seabuckthorn Leaves Enhances Rabies Virus Neutralizing Antibody Titers and CTL Response in Swiss Albino Mice

Jayashankar, B., Singh, D. K., Mishra, K. P., Madhusudana, S. N., & Ashwin, Y. (2016) · Journal of Vaccines and Immunology · doi:10.17352/jvi.000013 · Cited by 1

New Insights on the Adjuvant Properties of the Leishmania Infantum Eukaryotic Initiation Factor

Koutsoni, O. S., Barhoumi, M., Guizani, I., & Dotsika, E. (2021) · Vide Leaf, Hyderabad eBooks · doi:10.37247/paimmu2ed.2.2021.11 · Cited by 1

Cellular and molecular mechanisms of action of the novel adjuvant polyphosphazene

Awate, S. (2013) · University Library - University of Saskatchewan (University of Saskatchewan) · Cited by 1

Systemic Lupus Erythematosus Induced by Vaccines

Katz-Agranov, N. S., & Zandman‐Goddard, G. (2015) · doi:10.1002/9781118663721.ch22 · Cited by 1

Acute Disseminated Encephalomyelitis: Idiopathic, Post‐infectious, and Post‐vaccination

Karussis, D. M., & Petrou, P. (2015) · doi:10.1002/9781118663721.ch33 · Cited by 1

The role of dendritic cells in adjuvant-induced immune responses

Gustafsson, T. (2013) · Gothenburg University Publications Electronic Archive (Gothenburg University) · Cited by 1

Effect of arginine glutamate on protein aggregation in biopharmaceutical formulation

Kheddo, P. (2017) · Research Explorer (The University of Manchester) · Cited by 1

Monofosforil lipídeo A e diidrolipoil desidrogenase de Paracoccidioides brasiliensis têm efeito terapêutico na paracoccidiodomicose experimental

Landgraf, T. N. (2017) · doi:10.11606/t.17.2017.tde-06012017-165041 · Cited by 1

SV40 virus-like particles as an effective delivery system and a vaccine platform

Kawano, M., Matsui, M., & Handa, H. (2014) · doi:10.2217/fmeb2013.13.66 · Cited by 1

Combination nanoadjuvant-based vaccine against influenza virus for older adults

Senapati, S. (2020) · doi:10.31274/etd-20210114-134 · Cited by 1

Haemonchus contortus antigen identification and use of tropomyosin in ovine vaccine development

Russ, B. P. (2020) · doi:10.33915/etd.7944 · Cited by 1

Evaluation of IgG Avidity of Sera from Mice Immunized with RBD of SARS-CoV-2 or OMVs of Neisseria meningitidis by Immunoblot and Dot-BlotPreprint

Segati, A. F., da Costa, H. H. M., Prudêncio, C. R., Portilho, A. I., & Gaspari, E. D. (2023) · Preprints.org · doi:10.20944/preprints202312.2180.v1 · Cited by 1

Immunogenicity and safety of a live-attenuated SARS-CoV-2 vaccine candidate based on multiple attenuation mechanismsPreprint

Suzuki-Okutani, M., Okamura, S., Gis, T., Sasaki, H., Lee, S. P., Yoshida, A., Goto, S., Nakagawa, T., Ikawa, M., Kamitani, W., et al. (2024) · eLife · doi:10.7554/elife.97532.1 · Cited by 1

Immunogenicity and safety of a live-attenuated SARS-CoV-2 vaccine candidate based on multiple attenuation mechanismsPreprint

Suzuki-Okutani, M., Okamura, S., Tanggis, Sasaki, H., Lee, S. P., Yoshida, A., Goto, S., Matsumoto, M., Yamawaki, M., Miyazaki, T., et al. (2025) · eLife · doi:10.7554/elife.97532.2 · Cited by 1

Étude d'association des gènes impliqués dans l'activité du gène IL1R2 avec les phénotypes reliés à l'asthme /

Vaillancourt, V. T. (2012) · Constellation (Université du Québec à Chicoutimi) · doi:10.1522/030279331

Effect of Surface Chemistry on the Immune Responses and Cellular Interactions of Porous Silicon Nanoparticles

Shahbazi, M. (2015) · Työväentutkimus Vuosikirja

Caracterização e avaliação imunológica de três proteínas de superfície de Leptospira interrogans obtidas em Escherichia coli

Fernandes, L. G. V. (2013) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/d.87.2013.tde-08052013-111313

Development and evaluation of new therapeutic interventions for chronic hepatitis C virus infection

Holmström, F. (2015) · Figshare

Development of CTL-based liposomal vaccines

Uchida, T. (2010) · Drug Delivery System · doi:10.2745/dds.25.29

Highlights From The Latest Articles on Vaccine Development Using Nanoparticles

Ruwona, T. B., & Cui, Z. (2014) · Nanomedicine · doi:10.2217/nnm.14.176

L’ADN du soi, allié du système immunitaire pour la fonction adjuvante de l’alun

Marichal, T., Bureau, F., & Desmet, C. J. (2012) · médecine/sciences · doi:10.1051/medsci/2012281011

Physicochemical and biological characterisation of novel immunomodulators

Hubert, M. (2013) · Otago University Research Archive (University of Otago)

Mode of Adjuvant Action of the Nasally Delivered Cytokine Interleukin 1 Alpha

Thompson, A. L. (2011) · DukeSpace (Duke University)

SA-4-1BBL: A Novel Form of the 4-1BB Costimulatory Ligand as an Adjuvant Platform for the Development of Subunit Cancer Vaccines

Sharma, R. K., Srivastava, A. K., Zhao, H., Yolcu, E. S., & Shirwan, H. (2014) · Springer eBooks · doi:10.1007/978-3-7091-1818-4_12

Engineering the Extra Domain A of fibronectin as a vaccine adjuvant and study of its role in tissue regeneration

Julier, Z. (2015) · Infoscience (Ecole Polytechnique Fédérale de Lausanne) · doi:10.5075/epfl-thesis-6804

Utilization of a model vaccination system to evaluate the immunostimulatory characteristics of LicKM, a novel carrier molecule

Chabot, A. (2025) · Library, Museums and Press - UDSpace (University of Delaware) · doi:10.58088/ex5q-bt17

Clonotypic dominance within the HIV-epitope-specific T cell receptor repertoire correlates with phenotypic and functional impairment

Conrad, J. A. (2011)

Avaliação de adjuvantes como estratégia para aumentar a produção da vacina influenza no Instituto Butantan

de Freitas, F. A. (2015) · doi:10.11606/d.46.2015.tde-29092015-121836

Innate Immune Recognition of Conserved Structural Features of Bacterial Flagellin Shapes Host Antibody Responses

López-Yglesias, A. H. (2014) · ResearchWorks at the University of Washington (University of Washington)

Avaliação de diferentes vias de imunização com novo adjuvante para Neisseria meningitidis em diferentes linhagens de camundongos.

Brito, L. T. (2016) · doi:10.11606/d.87.2016.tde-10032016-102928

Skills, Knowledge, and Translational Technologies Leading to Novel Vaccines 1 The Immunological Fundamentals

Sefik, S. (2012)

Regulation of the germinal center response by T follicular helper cells and type I interferons

Dahlgren, M. W. (2016) · Lund University Publications (Lund University)

Avaliação de adjuvantes como estratégia para aumentar a produção da vacina influenza no Instituto Butantan

Paulo, S. (2015)

Nanomedicine: Implications from Nanotoxicity

Zhou, R. (2015) · Springer eBooks · doi:10.1007/978-3-319-15382-7_9

Síndroma Autoimune/Autoinflamatório induzido por Adjuvante - Síndroma ASIA ou de Shöenfeld

Ribeiro, D. A. M. (2013) · Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT) · doi:10.34626/1b7j-we70

Nanomedicine and Infection

Akagi, T., & Akashi, M. (2015) · Methods in pharmacology and toxicology · doi:10.1007/978-1-4939-3121-7_22

Resposta imune humoral em bovinos induzida pela glicoproteína D recombinante de herpesvírus bovino tipo 5

Araujo, I. L. (2014) · Americanae (AECID Library)

Exosomes : immunomodulators in cancer and therapy

Hiltbrunner, S. (2016) · Figshare

Vaccine Adjuvants

Reed, S. G., Orr, M. T., & Coler, R. N. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-802174-3.00004-7

Eosinophil Cell–Cell Communication

(2012) · Elsevier eBooks · doi:10.1016/b978-0-12-394385-9.00011-0

Aluminium Adjuvants – a Nanomaterial used as Adjuvants in Human Vaccines for Decades

Eriksson, H., Sandberg, T., & Danielsson, R. (2017) · Current Bionanotechnology · doi:10.2174/2213529403666170310143243 · Cited by 1

B cell fate following immunization : from memory B cells to plasma cells

Murillo, P. M. (2017) · Figshare

Papel de inflamassomas e vias lisossomais na morte celular e resposta imune induzidas pela flagelina.

Lage, S. L. (2016) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.42.2016.tde-25022016-095353

Filamentöz faj üzerinde eksperese edilen Hepatit B yüzey antijenine karşı antikor yanıtı

Başalp, A., HATİPOGLU, I. H., Balcıoğlu, B. K., Söğüt, İ., Bahadır, A. Ö., Uzyol, K. S., Sivas, H., & Erdağ, B. (2017) · Mehmet Akif Ersoy Üniversitesi Sağlık Bilimleri Enstitüsü Dergisi · doi:10.24998/maeusabed.322704

Adjuvant Interactions with Lipid Membranes and Their Effect on Cellular Immune Responses

Napolitano, L. R. A. (2017) · KU ScholarWorks (University of Kansas)

Utilização de peptídeo intracelular (EL28) como imunoestimulante da vacina de raiva.

Chipana, M. M. T. (2018) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/d.9.2018.tde-22012018-110104

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