Exploring immunotherapeutic strategies for bacterial and viral diseases

Ayodele Isaac Adedokun , Olaniyi Abideen Adigun , Adamu Muhammad Ibrahim , Ibrahim Idris , Paul Yiran Ntasin , Babatunde Ibrahim Olowu , Chinyere M. Ikele-Awaogu , Precious Kehinde Fadele , Ernesto Oluwafemi Dibia , Olalekan John Okesanya , Mohamed Mustaf Ahmed

Exploration of Immunology ›› 2025, Vol. 5 ›› Issue (1) : 1003202

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Exploration of Immunology ›› 2025, Vol. 5 ›› Issue (1) :1003202 DOI: 10.37349/ei.2025.1003202
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Exploring immunotherapeutic strategies for bacterial and viral diseases
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Abstract

The global socioeconomic and health impacts of microbial diseases cannot be overemphasized. The emergence of the coronavirus in 2019 and the ongoing threat of infectious diseases, such as HIV/AIDS, tuberculosis, and hepatitis, remind us of the impact these infections have on economic stability and global health. Gaps in the treatment of microbial infections and their contribution to increased mortality necessitate holistic and long-term solutions, as opposed to antibiotics, which were previously relied upon. Immunotherapy is becoming increasingly promising for the treatment of microbial infections. This study reviews recent advances in immunotherapeutic strategies, particularly cytokine-based therapies, adoptive cell therapy, monoclonal antibodies, and immune checkpoint inhibitors, for the control of antimicrobial resistance. New inventive approaches, such as chimeric antigen receptor T cell therapy and mucosal-associated invariant T cells, have been discussed in the context of bacterial and viral infections, highlighting promising results from clinical trials and addressing the challenges of toxicity, immune evasion, and therapy resistance that are inherent in these diseases. Future priorities include optimizing combination therapies and exploring new immunomodulatory targets to improve the effectiveness of these interventions in treating antimicrobial resistance and other infectious diseases.

Keywords

Coronavirus / immunotherapy / global health / microbial infections / diseases

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Ayodele Isaac Adedokun, Olaniyi Abideen Adigun, Adamu Muhammad Ibrahim, Ibrahim Idris, Paul Yiran Ntasin, Babatunde Ibrahim Olowu, Chinyere M. Ikele-Awaogu, Precious Kehinde Fadele, Ernesto Oluwafemi Dibia, Olalekan John Okesanya, Mohamed Mustaf Ahmed. Exploring immunotherapeutic strategies for bacterial and viral diseases. Exploration of Immunology, 2025, 5 (1) : 1003202 DOI:10.37349/ei.2025.1003202

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References

[1]

Antimicrobial Resistance Collaborators. Global burden of bacterial antimicrobial resistance in 2019: a systematic analysis. Lancet. 2022; 399: 629-55.

[2]

Haldar J. Confronting the Rising Threat of Antimicrobial Resistance: A Global Health Imperative. ACS Infect Dis. 2024; 10: 1-2.

[3]

World Health Organization. Antimicrobial resistance [Internet]. World Health Organization ; c2025 [cited 2025 Mar 25]. Available from: https://www.who.int/news-room/fact-sheets/detail/antimicrobial-resistance

[4]

Antimicrobial Resistance Facts and Stats [Internet]. U.S. Centers for Disease Control and Prevention; [cited 2025 May 9]. Available from: https://www.cdc.gov/antimicrobial-resistance/data-research/facts-stats/

[5]

New forecasts reveal that 39 million deaths will be directly attributable to bacterial antimicrobial resistance (AMR) between 2025-2050 [Internet]. Welcome; [cited 2025 May 9]. Available from: https://wellcome.org/news/new-forecasts-reveal-39-million-deaths-will-be-directly-attributable-bacterial-antimicrobial#top

[6]

Antimicrobial Resistance Threats in the United States, 2021-2022 [Internet]. U.S. Centers for Disease Control and Prevention; [cited 2024 Dec 30]. Available from: https://www.cdc.gov/antimicrobial-resistance/data-research/threats/update-2022.html

[7]

Muteeb G, Rehman MT, Shahwan M, Aatif M. Origin of Antibiotics and Antibiotic Resistance, and Their Impacts on Drug Development: A Narrative Review. Pharmaceuticals (Basel). 2023; 16: 1615.

[8]

Lobanovska M, Pilla G. Penicillin’s Discovery and Antibiotic Resistance: Lessons for the Future? Yale J Biol Med. 2017; 90: 135-45.

[9]

Baker RE, Mahmud AS, Miller IF, Rajeev M, Rasambainarivo F, Rice BL, et al. Infectious disease in an era of global change. Nat Rev Microbiol. 2022; 20: 193-205.

[10]

Mir MA, Hamdani SS, Qadri H. Significance of immunotherapy for human bacterial diseases and antibacterial drug discovery. In: Mir MA, editor. Human Pathogenic Microbes. Academic Press; 2022. pp. 129-61.

[11]

cytokine [Internet]. Encyclopædia Britannica, Inc.; c2025 [cited 2024 Nov 20]. Available from: https://www.britannica.com/science/cytokine

[12]

Petrina M, Martin J, Basta S. Granulocyte macrophage colony-stimulating factor has come of age: From a vaccine adjuvant to antiviral immunotherapy. Cytokine Growth Factor Rev. 2021; 59: 101-10.

[13]

Chuang Y, He L, Pinn ML, Tsai Y, Cheng MA, Farmer E, et al. Albumin fusion with granulocyte-macrophage colony-stimulating factor acts as an immunotherapy against chronic tuberculosis. Cell Mol Immunol. 2021; 18: 2393-401.

[14]

Sheng L, Li X, Weng F, Wu S, Chen Y, Lou L. Efficacy and Safety of Adjunctive Recombinant Human Interleukin-2 for Patients with Pulmonary Tuberculosis: A Meta-Analysis. J Trop Med. 2022; 2022: 5071816.

[15]

Karki R, Kanneganti T. The ‘cytokine storm’: molecular mechanisms and therapeutic prospects. Trends Immunol. 2021; 42: 681-705.

[16]

Khanna NR, Gerriets V. Interferon. Treasure Island (FL): StatPearls Publishing; 2025.

[17]

Calabrese LH, Lenfant T, Calabrese C. Interferon therapy for COVID-19 and emerging infections: Prospects and concerns. Cleve Clin J Med. 2020.

[18]

Gunst JD, Goonetilleke N, Rasmussen TA, Søgaard OS. Immunomodulation with IL-7 and IL-15 in HIV-1 infection. J Virus Erad. 2023; 9: 100347.

[19]

Morillas RM, Masnou H, Ardévol M, López D. Role of ribavirin in interferon-free therapy for the treatment of hepatitisC virus. Gastroenterol Hepatol. 2017; 40: 699-708.

[20]

Wagoner J, Herring S, Hsiang T, Ianevski A, Biering SB, Xu S, et al. Combinations of Host- and Virus-Targeting Antiviral Drugs Confer Synergistic Suppression of SARS-CoV-2. Microbiol Spectr. 2022; 10: e0333122.

[21]

Bojkova D, Stack R, Rothenburger T, Kandler JD, Ciesek S, Wass MN, et al. Synergism of interferon-beta with antiviral drugs against SARS-CoV-2 variants. J Infect. 2022; 85: 573-607.

[22]

Choi MH, Wan EYF, Wong ICK, Chan EWY, Chu WM, Tam AR, et al. Comparative effectiveness of combination therapy with nirmatrelvir-ritonavir and remdesivir versus monotherapy with remdesivir or nirmatrelvir-ritonavir in patients hospitalised with COVID-19: a target trial emulation study. Lancet Infect Dis. 2024; 24: 1213- 24.

[23]

Aliyu M, Zohora FT, Anka AU, Ali K, Maleknia S, Saffarioun M, et al. Interleukin-6 cytokine: An overview of the immune regulation, immune dysregulation, and therapeutic approach. Int Immunopharmacol. 2022; 111: 109130.

[24]

Cytokine Release Syndrome [Internet]. WebMD LLC; c1994- 2025 [cited 2024 Dec 10]. Available from: https://emedicine.medscape.com/article/2500111-overview

[25]

Deckers J, Anbergen T, Hokke AM, de Dreu A, Schrijver DP, de Bruin K, et al. Engineering cytokine therapeutics. Nat Rev Bioeng. 2023; 1: 286-303.

[26]

Pires IS, Hammond PT, Irvine DJ. Engineering Strategies for Immunomodulatory Cytokine Therapies - Challenges and Clinical Progress. Adv Ther (Weinh). 2021; 4: 2100035.

[27]

Gubser C, Chiu C, Lewin SR, Rasmussen TA. Immune checkpoint blockade in HIV. EBioMedicine. 2022; 76: 103840.

[28]

Shah NJ, Pia AD, Wu T, Williams A, Weber M, Sinclaire B, et al. Clinical Outcomes of Immune Checkpoint Inhibitors in Unique Cohorts Underrepresented in Clinical Trials. Cancers (Basel). 2024; 16: 2223.

[29]

Wykes MN, Lewin SR. Immune checkpoint blockade in infectious diseases. Nat Rev Immunol. 2018; 18: 91-104.

[30]

Vance RE, Eichberg MJ, Portnoy DA, Raulet DH. Listening to each other: Infectious disease and cancer immunology. Sci Immunol. 2017; 2: eaai9339.

[31]

Saeidi A, Zandi K, Cheok YY, Saeidi H, Wong WF, Lee CYQ, et al. T-Cell Exhaustion in Chronic Infections: Reversing the State of Exhaustion and Reinvigorating Optimal Protective Immune Responses. Front Immunol. 2018; 9: 2569.

[32]

Cao H, Zhang R, Zhang W. CTLA4 interferes with the HBV-specific T cell immune response (Review). Int J Mol Med. 2018; 42: 703-12.

[33]

Jubel JM, Barbati ZR, Burger C, Wirtz DC, Schildberg FA. The Role of PD-1 in Acute and Chronic Infection. Front Immunol. 2020; 11: 487.

[34]

Fromentin R, DaFonseca S, Costiniuk CT, El-Far M, Procopio FA, Hecht FM, et al. PD-1 blockade potentiates HIV latency reversal ex vivo in CD4+ T cells from ART-suppressed individuals . Nat Commun. 2019; 10: 814.

[35]

Van der Sluis RM, Kumar NA, Pascoe RD, Zerbato JM, Evans VA, Dantanarayana AI, et al. Combination Immune Checkpoint Blockade to Reverse HIV Latency. J Immunol. 2020; 204: 1242-54.

[36]

Lewis PE, Poteet EC, Liu D, Chen C, LaBranche CC, Stanfield-Oakley SA, et al. CTLA-4 Blockade, during HIV Virus-Like Particles Immunization, Alters HIV-Specific B-Cell Responses. Vaccines (Basel). 2020; 8: 284.

[37]

Mellinghoff SC, Vanshylla K, Dahlke C, Addo MM, Cornely OA, Klein F, et al. Case Report: Clinical Management of a Patient With Metastatic Non-Small Cell Lung Cancer Newly Receiving Immune Checkpoint Inhibition During Symptomatic COVID-19. Front Immunol. 2021; 12: 798276.

[38]

Pan Y, Tan J, Li J, Li T, Li J, Cao Y, et al. Immune checkpoint inhibitors in cancer patients with COVID-19. Open Life Sci. 2023; 18: 20220641.

[39]

Karsten H, Matrisch L, Cichutek S, Fiedler W, Alsdorf W, Block A. Broadening the horizon: potential applications of CAR-T cells beyond current indications. Front Immunol. 2023; 14: 1285406.

[40]

Ogishi M, Yang R, Aytekin C, Langlais D, Bourgey M, Khan T, et al. Inherited PD-1 deficiency underlies tuberculosis and autoimmunity in a child. Nat Med. 2021; 27: 1646-54.

[41]

Barber DL, Sakai S, Kudchadkar RR, Fling SP, Day TA, Vergara JA, et al. Tuberculosis following PD-1 blockade for cancer immunotherapy. Sci Transl Med. 2019; 11: eaat2702.

[42]

Chiu CY, Chang JJ, Dantanarayana AI, Solomon A, Evans VA, Pascoe R, et al. Combination Immune Checkpoint Blockade Enhances IL-2 and CD107a Production from HIV-Specific T Cells Ex Vivo in People Living with HIV on Antiretroviral Therapy. J Immunol. 2022; 208: 54-62.

[43]

Hsu C, Lee S, Ejadi S, Even C, Cohen RB, Tourneau CL, et al. Safety and Antitumor Activity of Pembrolizumab in Patients With Programmed Death-Ligand 1-Positive Nasopharyngeal Carcinoma: Results of the KEYNOTE-028 Study. J Clin Oncol. 2017; 35: 4050-6.

[44]

Fang W, Yang Y, Ma Y, Hong S, Lin L, He X, et al. Camrelizumab (SHR-1210) alone or in combination with gemcitabine plus cisplatin for nasopharyngeal carcinoma: results from two single-arm, phase 1 trials. Lancet Oncol. 2018; 19: 1338-50.

[45]

Fuchs CS, Doi T, Jang RW, Muro K, Satoh T, Machado M, et al. Safety and Efficacy of Pembrolizumab Monotherapy in Patients With Previously Treated Advanced Gastric and Gastroesophageal Junction Cancer: Phase 2 Clinical KEYNOTE-059 Trial. JAMA Oncol. 2018; 4: e180013.

[46]

Gay CL, Bosch RJ, McKhann A, Moseley KF, Wimbish CL, Hendrickx SM, et al. Suspected Immune-Related Adverse Events With an Anti-PD-1 Inhibitor in Otherwise Healthy People With HIV. J Acquir Immune Defic Syndr. 2021; 87: e234-6.

[47]

Cai X, Zhan H, Ye Y, Yang J, Zhang M, Li J, et al. Current Progress and Future Perspectives of Immune Checkpoint in Cancer and Infectious Diseases. Front Genet. 2021; 12: 785153.

[48]

Yan J, Yang L, Ren Q, Zhu C, Du H, Wang Z, et al. Gut microbiota as a biomarker and modulator of anti-tumor immunotherapy outcomes. Front Immunol. 2024; 15: 1471273.

[49]

Lin A, Jiang A, Huang L, Li Y, Zhang C, Zhu L, et al. From chaos to order: optimizing fecal microbiota transplantation for enhanced immune checkpoint inhibitors efficacy. Gut Microbes. 2025; 17: 2452277.

[50]

Fan J, Jin S, Gilmartin L, Toth I, Hussein WM, Stephenson RJ. Advances in Infectious Disease Vaccine Adjuvants. Vaccines (Basel). 2022; 10: 1120.

[51]

Zhao T, Cai Y, Jiang Y, He X, Wei Y, Yu Y, et al. Vaccine adjuvants: mechanisms and platforms. Signal Transduct Target Ther. 2023; 8: 283.

[52]

Manriquez GGG, Tuero I. Adjuvants: friends in vaccine formulations against infectious diseases. Hum Vaccin Immunother. 2021; 17: 3539-50.

[53]

Crothers JW, Norton EB. Recent advances in enterotoxin vaccine adjuvants. Curr Opin Immunol. 2023; 85: 102398.

[54]

Verbeke R, Hogan MJ, Loré K, Pardi N. Innate immune mechanisms of mRNA vaccines. Immunity. 2022; 55: 1993-2005.

[55]

Kutikuppala LVS, Kourampi I, Kanagala RSD, Bhattacharjee P, Boppana SH. Prospects and Challenges in Developing mRNA Vaccines for Infectious Diseases and Oncogenic Viruses. Med Sci (Basel). 2024; 12: 28.

[56]

Adjuvants and Vaccines [Internet]. U.S. Centers for Disease Control and Prevention; [cited 2025 Feb 25]. Available from: https://www.cdc.gov/vaccine-safety/about/adjuvants.html?CDC_AAref_Val=https://www.cdc.gov/vaccinesafety/concerns/adjuvants.html

[57]

Kayesh MEH, Kohara M, Tsukiyama-Kohara K. TLR agonists as vaccine adjuvants in the prevention of viral infections: an overview. Front Microbiol. 2023; 14: 1249718.

[58]

Khlebnikova A, Kirshina A, Zakharova N, Ivanov R, Reshetnikov V. Current Progress in the Development of mRNA Vaccines Against Bacterial Infections. Int J Mol Sci. 2024; 25: 13139.

[59]

Muslimov A, Tereshchenko V, Shevyrev D, Rogova A, Lepik K, Reshetnikov V, et al. The Dual Role of the Innate Immune System in the Effectiveness of mRNA Therapeutics. Int J Mol Sci. 2023; 24: 14820.

[60]

Vasileva OO, Tereschenko VP, Krapivin BN, Muslimov AR, Kukushkin IS, Pateev II, et al. Immunogenicity of full-length and multi-epitope mRNA vaccines for M. Tuberculosis as demonstrated by the intensity of T-cell response: a comparative study in mice . Bull Russ State Med Univ. 2023: 42-8.

[61]

van den Berg RA, De Mot L, Leroux-Roels G, Bechtold V, Clement F, Coccia M, et al. Adjuvant-Associated Peripheral Blood mRNA Profiles and Kinetics Induced by the Adjuvanted Recombinant Protein Candidate Tuberculosis Vaccine M72/AS01 in Bacillus Calmette-Guérin-Vaccinated Adults. Front Immunol. 2018; 9: 564.

[62]

World Health Organization. Pfizer-BioNTech COVID-19 Vaccine, COMIRNATY® (Tozinameran). World Health Organization ; 2022.

[63]

Loomis RJ, DiPiazza AT, Falcone S, Ruckwardt TJ, Morabito KM, Abiona OM, et al. Chimeric Fusion (F) and Attachment (G) Glycoprotein Antigen Delivery by mRNA as a Candidate Nipah Vaccine. Front Immunol. 2021; 12: 772864.

[64]

Larsen SE, Erasmus JH, Reese VA, Pecor T, Archer J, Kandahar A, et al. An RNA-Based Vaccine Platform for Use against Mycobacterium tuberculosis . Vaccines (Basel). 2023; 11: 130.

[65]

Sajid A, Matias J, Arora G, Kurokawa C, DePonte K, Tang X, et al. mRNA vaccination induces tick resistance and prevents transmission of the Lyme disease agent. Sci Transl Med. 2021; 13: eabj9827.

[66]

SPIKEVAX [Internet]. U.S. Food and Drug Administration; [cited 2025 May 7]. Available from: https://www.fda.gov/vaccines-blood-biologics/spikevax

[67]

Baden LR, El Sahly HM, Essink B, Kotloff K, Frey S, Novak R, et al. Efficacy and Safety of the mRNA-1273 SARS-CoV-2 Vaccine. N Engl J Med. 2021; 384: 403-16.

[68]

Wilson B, Geetha KM. Lipid nanoparticles in the development of mRNA vaccines for COVID-19. J Drug Deliv Sci Technol. 2022; 74: 103553.

[69]

Feldman RA, Fuhr R, Smolenov I, Ribeiro AM, Panther L, Watson M, et al. mRNA vaccines against H10N8 and H7N9 influenza viruses of pandemic potential are immunogenic and well tolerated in healthy adults in phase 1 randomized clinical trials. Vaccine. 2019; 37: 3326-34.

[70]

Wang X, Liu C, Rcheulishvili N, Papukashvili D, Xie F, Zhao J, et al. Strong immune responses and protection of PcrV and OprF-I mRNA vaccine candidates against Pseudomonas aeruginosa . NPJ Vaccines. 2023; 8: 76.

[71]

Kawaguchi K, Kinoshita M, Sudo K, Inoue K, Naito Y, Oba M, et al. mRNA vaccine induces protective immunity against the type III secretory virulence of Pseudomonas aeruginosa . bioRxiv 2023.06.09.544431 [Preprint]. 2023 [cited 2024 Nov 20]. Available from: https://doi.org/10.1101/2023.06.09.544431

[72]

Verbeke R, Lentacker I, Breckpot K, Janssens J, Calenbergh SV, Smedt SCD, et al. Broadening the Message: A Nanovaccine Co-loaded with Messenger RNA and α-GalCer Induces Antitumor Immunity through Conventional and Natural Killer T Cells. ACS Nano. 2019; 13: 1655-69.

[73]

Corbett KS, Flynn B, Foulds KE, Francica JR, Boyoglu-Barnum S, Werner AP, et al. Evaluation of the mRNA-1273 Vaccine against SARS-CoV-2 in Nonhuman Primates. N Engl J Med. 2020; 383: 1544-55.

[74]

Chaudhary N, Weissman D, Whitehead KA. mRNA vaccines for infectious diseases: principles, delivery and clinical translation. Nat Rev Drug Discov. 2021; 20: 817-38.

[75]

Kose N, Fox JM, Sapparapu G, Bombardi R, Tennekoon RN, de Silva AD, et al. A lipid-encapsulated mRNA encoding a potently neutralizing human monoclonal antibody protects against chikungunya infection. Sci Immunol. 2019; 4: eaaw6647.

[76]

Dasari V, McNeil LK, Beckett K, Solomon M, Ambalathingal G, Thuy TL, et al. Lymph node targeted multi-epitope subunit vaccine promotes effective immunity to EBV in HLA-expressing mice. Nat Commun. 2023; 14: 4371.

[77]

Wang J, Wang R, Wang M, Ge J, Wang Y, Li Y, et al. Cutting-Edge Therapy and Immune Escape Mechanisms in EBV-Associated Tumors. Med Res Rev. 2025; 45: 1184-210.

[78]

Guo X, Liu D, Huang Y, Deng Y, Wang Y, Mao J, et al. Revolutionizing viral disease vaccination: the promising clinical advancements of non-replicating mRNA vaccines. Virol J. 2023; 20: 64.

[79]

Bu W, Joyce MG, Nguyen H, Banh DV, Aguilar F, Tariq Z, et al. Immunization with Components of the Viral Fusion Apparatus Elicits Antibodies That Neutralize Epstein-Barr Virus in B Cells and Epithelial Cells. Immunity. 2019; 50: 1305-16.e6.

[80]

Mortazavi B, Molaei A, Fard NA. Multi-epitopevaccines, from design to expression; an in silico approach. Hum Immunol. 2024; 85: 110804.

[81]

Thrift WJ, Perera J, Cohen S, Lounsbury NW, Gurung HR, Rose CM, et al. Graph-pMHC: graph neural network approach to MHC class II peptide presentation and antibody immunogenicity. Brief Bioinform. 2024; 25: bbae123.

[82]

Albert BA, Yang Y, Shao XM, Singh D, Smit KN, Anagnostou V, et al. Deep neural networks predict class I major histocompatibility complex epitope presentation and transfer learn neoepitope immunogenicity. Nat Mach Intell. 2023; 5: 861-72.

[83]

Parvizpour S, Pourseif MM, Razmara J, Rafi MA, Omidi Y. Epitope-based vaccine design: a comprehensive overview of bioinformatics approaches. Drug Discov Today. 2020; 25: 1034-42.

[84]

Monoclonal antibodies (mAbs) [Internet]. Cancer Research UK; [cited 2025 Feb 20]. Available from: https://www.cancerresearchuk.org/about-cancer/treatment/targeted-cancer-drugs-immunotherapy/monoclonal-antibodies

[85]

Esposito S, Amirthalingam G, Bassetti M, Blasi F, Rosa FGD, Halasa NB, et al. Monoclonal antibodies for prophylaxis and therapy of respiratory syncytial virus, SARS-CoV-2, human immunodeficiency virus, rabies and bacterial infections: an update from the World Association of Infectious Diseases and Immunological Disorders and the Italian Society of Antinfective Therapy. Front Immunol. 2023; 14: 1162342.

[86]

Motley MP, Banerjee K, Fries BC. Monoclonal antibody-based therapies for bacterial infections. Curr Opin Infect Dis. 2019; 32: 210-6.

[87]

Iqbal T, Choudhary P, Raza K. Monoclonal Antibodies in Cancer Therapy. Int J Multidiscip Res. 2023; 5.

[88]

Monoclonal Antibodies and Their Side Effects [Internet]. American Cancer Society, Inc.; c2025 [cited 2025 May 5]. Available from: https://www.cancer.org/cancer/managing-cancer/treatment-types/immunotherapy/monoclonal-antibodies.html

[89]

Pantaleo G, Correia B, Fenwick C, Joo VS, Perez L. Antibodies to combat viral infections: development strategies and progress. Nat Rev Drug Discov. 2022; 21: 676-96.

[90]

Otsubo R, Yasui T. Monoclonal antibody therapeutics for infectious diseases: Beyond normal human immunoglobulin. Pharmacol Ther. 2022; 240: 108233.

[91]

Makari D, Jensen KM, Harris B, Jafri HS. Randomized, Double-Blind Study of the Safety of the Liquid Versus Lyophilized Formulation of Palivizumab in Premature Infants and Children with Chronic Lung Disease of Prematurity. Infect Dis Ther. 2014; 3: 339-47.

[92]

Brookes RH, Ming M, Williams K, Hopfer R, Gurunathan S, Gallichan S, et al. Passive protection of mice against Streptococcus pneumoniae challenge by naturally occurring and vaccine-induced human anti-PhtD antibodies. Hum Vaccin Immunother. 2015; 11: 1836-9.

[93]

Ali SO, Yu XQ, Robbie GJ, Wu Y, Shoemaker K, Yu L, et al. Phase 1 study of MEDI3902, an investigational anti- Pseudomonas aeruginosa PcrV and Psl bispecific human monoclonal antibody, in healthy adults . Clin Microbiol Infect. 2019; 25: 629.e1-6.

[94]

François B, Mercier E, Gonzalez C, Asehnoune K, Nseir S, Fiancette M, et al. Safety and tolerability of a single administration of AR-301, a human monoclonal antibody, in ICU patients with severe pneumonia caused by Staphylococcus aureus: first-in-human trial . Intensive Care Med. 2018; 44: 1787-96.

[95]

Varshney AK, Kuzmicheva GA, Lin J, Sunley KM, Bowling RA Jr, Kwan T, et al. A natural human monoclonal antibody targeting Staphylococcus Protein A protects against Staphylococcus aureus bacteremia . PLoS One. 2018; 13: e0190537.

[96]

Esposito S, Abu-Raya B, Bonanni P, Cahn-Sellem F, Flanagan KL, Torres FM, et al. Coadministration of Anti-Viral Monoclonal Antibodies With Routine Pediatric Vaccines and Implications for Nirsevimab Use: A White Paper. Front Immunol. 2021; 12: 708939.

[97]

Clesrovimab in Infants and Children at Increased Risk for Severe Respiratory Syncytial Virus Disease [Internet]. Rahway: Merck & Co., Inc.; c2025 [cited 2025 May 8]. Available from: https://www.merckclinicaltrials.com/trial/nct04938830/

[98]

Coronavirus (COVID-19) Update: FDA Authorizes Additional Monoclonal Antibody for Treatment of COVID-19 2021 [Internet]. U.S. Food and Drug Administration; [cited 2024 Oct 10]. Available from: https://www.fda.gov/news-events/press-announcements/coronavirus-covid-19-update-fda-authorizes-additional-monoclonal-antibody-treatment-covid-19#:~:text=Today%2C%20the%20U.S.%20Food%20and,about%2088%20pounds%5D)%20with

[99]

Mazumdar S. Raxibacumab. MAbs. 2009; 1: 531-8.

[100]

Johnson S, Gerding DN. Bezlotoxumab. Clin Infect Dis. 2019; 68: 699-704.

[101]

Greig SL. Obiltoxaximab: First Global Approval. Drugs. 2016; 76: 823-30.

[102]

Kansagra K, Parmar D, Mendiratta SK, Patel J, Joshi S, Sharma N, et al. A Phase 3, Randomized, Open-label, Noninferiority Trial Evaluating Anti-Rabies Monoclonal Antibody Cocktail (Twinrab) Against Human Rabies Immunoglobulin (HRIG) . Clin Infect Dis. 2021; 73: e2722-8.

[103]

Fan L, Zhang L, Li J, Zhu F. Advances in the progress of monoclonal antibodies for rabies. Hum Vaccin Immunother. 2022; 18: 2026713.

[104]

Beccari MV, Mogle BT, Sidman EF, Mastro KA, Asiago-Reddy E, Kufel WD. Ibalizumab, a Novel Monoclonal Antibody for the Management of Multidrug-Resistant HIV-1 Infection. Antimicrob Agents Chemother. 2019; 63: e00110-19.

[105]

FDA approves new HIV treatment for patients who have limited treatment options [Internet]. U.S. Food and Drug Administration ; [cited 2025 May 9]. Available from: https://www.natap.org/2018/CROI/croi_36.htm#:~:text=%22Trogarzo%20is%20the%20first%20drug%20in%20a,have%20run%20out%20of%20HIV%20treatment%20options.&text=A%20significant%20decrease%20in%20viral%20load%20after,to%20their%20failing%20ART%20(or%20no%20therapy)

[106]

Zahavi D, Weiner L. Monoclonal Antibodies in Cancer Therapy. Antibodies (Basel). 2020; 9: 34.

[107]

Ranzani OT, Forte DN, Forte AC, Mimica I, Forte WCN. The value of antibody-coated bacteria in tracheal aspirates for the diagnosis of ventilator-associated pneumonia: a case-control study. J Bras Pneumol. 2016; 42: 203-10.

[108]

Crowe JE Jr. Human Antibodies for Viral Infections. Annu Rev Immunol. 2022; 40: 349-86.

[109]

Walti CS, Stuehler C, Palianina D, Khanna N. Immunocompromised host section: Adoptive T-cell therapy for dsDNA viruses in allogeneic hematopoietic cell transplant recipients. Curr Opin Infect Dis. 2022; 35: 302-11.

[110]

Morte-Romea E, Pesini C, Pellejero-Sagastizábal G, Letona-Giménez S, Martínez-Lostao L, Aranda SL, et al. CAR Immunotherapy for the treatment of infectious diseases: a systematic review. Front Immunol. 2024; 15: 1289303.

[111]

Koukoulias K, Papayanni PG, Leen AM, Vasileiou S. Virus-Specific T-Cell Therapy for the Management of Viral Infections in the Immunocompromised. Transfus Med Hemother. 2024; 52: 5-26.

[112]

Keller MD, Hanley PJ, Chi Y, Aguayo-Hiraldo P, Dvorak CC, Verneris MR, et al. Antiviral cellular therapy for enhancing T-cell reconstitution before or after hematopoietic stem cell transplantation (ACES): a two-arm, open label phase II interventional trial of pediatric patients with risk factor assessment. Nat Commun. 2024; 15: 3258.

[113]

Pfeiffer T, Tzannou I, Wu M, Ramos C, Sasa G, Martinez C, et al. Posoleucel, an Allogeneic, Off-the-Shelf Multivirus-Specific T-Cell Therapy, for the Treatment of Refractory Viral Infections in the Post-HCT Setting. Clin Cancer Res. 2023; 29: 324-30.

[114]

Mahadeo KM, Baiocchi R, Beitinjaneh A, Chaganti S, Choquet S, Dierickx D, et al. Tabelecleucel for allogeneic haematopoietic stem-cell or solid organ transplant recipients with Epstein-Barr virus-positive post-transplant lymphoproliferative disease after failure of rituximab or rituximab and chemotherapy (ALLELE): a phase 3, multicentre, open-label trial. Lancet Oncol. 2024; 25: 376-87.

[115]

Seif M, Einsele H, Löffler J. CAR T Cells Beyond Cancer: Hope for Immunomodulatory Therapy of Infectious Diseases. Front Immunol. 2019; 10: 2711.

[116]

Rothemejer FH, Lauritsen NP, Søgaard OS, Tolstrup M. Strategies for enhancing CAR T cell expansion and persistence in HIV infection. Front Immunol. 2023; 14: 1253395.

[117]

Mazzi MT, Hajdu KL, Ribeiro PR, Bonamino MH. CAR-T cells leave the comfort zone: current and future applications beyond cancer. Immunother Adv. 2020; 1: ltaa006.

[118]

Zmievskaya E, Valiullina A, Ganeeva I, Petukhov A, Rizvanov A, Bulatov E. Application of CAR-T Cell Therapy beyond Oncology: Autoimmune Diseases and Viral Infections. Biomedicines. 2021; 9: 59.

[119]

Maldini CR, Ellis GI, Riley JL. CAR T cells for infection, autoimmunity and allotransplantation. Nat Rev Immunol. 2018; 18: 605-16.

[120]

Schreiber S, Dressler LS, Loffredo-Verde E, Asen T, Färber S, Wang W, et al. CARs derived from broadly neutralizing, human monoclonal antibodies identified by single B cell sorting target hepatitis B virus-positive cells. Front Immunol. 2024; 15: 1340619.

[121]

Kalinina AA, Nesterenko LN, Bruter AV, Balunets DV, Chudakov DM, Izraelson M, et al. Adoptive Immunotherapy Based on Chain-Centric TCRs in Treatment of Infectious Diseases. iScience. 2020; 23: 101854.

[122]

Tacke R, Sun J, Uchiyama S, Polovina A, Nguyen DG, Nizet V. Protection Against Lethal Multidrug-Resistant Bacterial Infections Using Macrophage Cell Therapy. Infect Microbes Dis. 2019; 1: 61-9.

[123]

Wang Z, Wu A, Cheng W, Li Y, Li D, Wang L, et al. Adoptive macrophage directed photodynamic therapy of multidrug-resistant bacterial infection. Nat Commun. 2023; 14: 7251.

[124]

Chung YR, Dangi T, Palacio N, Sanchez S, Penaloza-MacMaster P. Adoptive B cell therapy for chronic viral infection. Front Immunol. 2022; 13: 908707.

[125]

Institute for Quality and Efficiency in Health Care: Executive Summaries. Cologne: Institute for Quality and Efficiency in Health Care (IQWiG); 2005.

[126]

Kaer LV, Parekh VV, Wu L. Invariant natural killer T cells: bridging innate and adaptive immunity. Cell Tissue Res. 2011; 343: 43-55.

[127]

Jeong D, Woo YD, Chung DH. Invariant natural killer T cells in lung diseases. Exp Mol Med. 2023; 55: 1885-94.

[128]

Wu L, Kaer LV. Natural killer T cells in health and disease. Front Biosci (Schol Ed). 2011; 3: 236-51.

[129]

Al-Qahtani AA, Alhamlan FS, Al-Qahtani AA. Pro-Inflammatory and Anti-Inflammatory Interleukins in Infectious Diseases: A Comprehensive Review. Trop Med Infect Dis. 2024; 9: 13.

[130]

Jin Y, Tan Y, Wu J, Ren Z. Lipid droplets: a cellular organelle vital in cancer cells. Cell Death Discov. 2023; 9: 254.

[131]

Zhang P, Lee JS, Gartlan KH, Schuster IS, Comerford I, Varelias A, et al. Eomesodermin promotes the development of type 1 regulatory T (TR1) cells . Sci Immunol. 2017; 2: eaah7152.

[132]

Batista IA, Quintas ST, Melo SA. The Interplay of Exosomes and NK Cells in Cancer Biology. Cancers (Basel). 2021; 13: 473.

[133]

Razizadeh MH, Zafarani A, Taghavi-Farahabadi M, Khorramdelazad H, Minaeian S, Mahmoudi M. Natural killer cells and their exosomes in viral infections and related therapeutic approaches: where are we? Cell Commun Signal. 2023; 21: 261.

[134]

Wen C, Seeger RC, Fabbri M, Wang L, Wayne AS, Jong AY. Biological roles and potential applications of immune cell-derived extracellular vesicles. J Extracell Vesicles. 2017; 6: 1400370.

[135]

Sada-Ovalle I, Chiba A, Gonzales A, Brenner MB, Behar SM. Innate invariant NKT cells recognize Mycobacterium tuberculosis-infected macrophages, produce interferon-gamma, and kill intracellular bacteria. PLoS Pathog. 2008; 4: e1000239.

[136]

Chaudhari P, Ghate V, Nampoothiri M, Lewis S. Multifunctional role of exosomes in viral diseases: From transmission to diagnosis and therapy. Cell Signal. 2022; 94: 110325.

[137]

Fiore PF, Pace ALD, Conti LA, Tumino N, Besi F, Scaglione S, et al. Different effects of NK cells and NK-derived soluble factors on cell lines derived from primary or metastatic pancreatic cancers. Cancer Immunol Immunother. 2023; 72: 1417-28.

[138]

Hatami Z, Hashemi ZS, Eftekhary M, Amiri A, Karpisheh V, Nasrollahi K, et al. Natural killer cell-derived exosomes for cancer immunotherapy: innovative therapeutics art. Cancer Cell Int. 2023; 23: 157.

[139]

Prokopeva AE, Emene CC, Gomzikova MO. Antitumor Immunity: Role of NK Cells and Extracellular Vesicles in Cancer Immunotherapy. Curr Issues Mol Biol. 2023; 46: 140-52.

[140]

Wang MM, Coupland SE, Aittokallio T, Figueiredo CR. Resistance to immune checkpoint therapies by tumour-induced T-cell desertification and exclusion: key mechanisms, prognostication and new therapeutic opportunities. Br J Cancer. 2023; 129: 1212-24.

[141]

Liu Y, Wang G, Chai D, Dang Y, Zheng J, Li H. iNKT: A new avenue for CAR-based cancer immunotherapy. Transl Oncol. 2022; 17: 101342.

[142]

Tognarelli EI, Gutiérrez-Vera C, Palacios PA, Pasten-Ferrada IA, Aguirre-Muñoz F, Cornejo DA, et al. Natural Killer T Cell Diversity and Immunotherapy. Cancers (Basel). 2023; 15: 5737.

[143]

Hu Y, Hu Q, Li Y, Lu L, Xiang Z, Yin Z, et al. γδ T cells: origin and fate, subsets, diseases and immunotherapy. Signal Transduct Target Ther. 2023; 8: 434.

[144]

Wang Y, Xu Y, Chen H, Zhang J, He W. Novel insights based on the plasticity of γδ T cells in the tumor microenvironment. Explor Immunol. 2022; 2: 98-132.

[145]

Revesz IA, Joyce P, Ebert LM, Prestidge CA. Effective γδ T-cell clinical therapies: current limitations and future perspectives for cancer immunotherapy. Clin Transl Immunology. 2024; 13: e1492.

[146]

Godfrey DI, Koay H, McCluskey J, Gherardin NA. The biology and functional importance of MAIT cells. Nat Immunol. 2019; 20: 1110-28.

[147]

Rouxel O, Lehuen A. Mucosal-associated invariant T cells in autoimmune and immune-mediated diseases. Immunol Cell Biol. 2018; 96: 618-29.

[148]

Corbett AJ, Awad W, Wang H, Chen Z. Antigen Recognition by MR1-Reactive T Cells; MAIT Cells, Metabolites, and Remaining Mysteries. Front Immunol. 2020; 11: 1961.

[149]

Hinks TSC, Zhang X. MAIT Cell Activation and Functions. Front Immunol. 2020; 11: 1014.

[150]

Aboagye EO, Bhujwalla ZM. Malignant transformation alters membrane choline phospholipid metabolism of human mammary epithelial cells. Cancer Res. 1999; 59: 80-4.

[151]

Nel I, Bertrand L, Toubal A, Lehuen A. MAIT cells, guardians of skin and mucosa? Mucosal Immunol. 2021; 14: 803- 14.

[152]

Leeansyah E, Boulouis C, Kwa ALH, Sandberg JK. Emerging Role for MAIT Cells in Control of Antimicrobial Resistance. Trends Microbiol. 2021; 29: 504-16.

[153]

Gherardin NA, Souter MN, Koay H, Mangas KM, Seemann T, Stinear TP, et al. Human blood MAIT cell subsets defined using MR1 tetramers. Immunol Cell Biol. 2018; 96: 507-25.

[154]

Liu Y, Wang W, Wu X, Weng X. Detection, Expansion, and Isolation of Human MAIT Cells. Methods Mol Biol. 2020; 2111: 285-93.

[155]

Sortino O, Richards E, Dias J, Leeansyah E, Sandberg JK, Sereti I. IL-7 treatment supports CD8+ mucosa-associated invariant T-cell restoration in HIV-1-infected patients on antiretroviral therapy. AIDS. 2018; 32: 825-8.

[156]

Siefert AL, Fahmy TM, Kim D. Artificial Antigen-Presenting Cells for Immunotherapies. Methods Mol Biol. 2017; 1530: 343-53.

[157]

Krawic JR, Ladd NA, Cansler M, McMurtrey C, Devereaux J, Worley A, et al. Multiple Isomers of Photolumazine V Bind MR1 and Differentially Activate MAIT Cells. J Immunol. 2024; 212: 933-40.

[158]

Leeansyah E, Ganesh A, Quigley MF, Sönnerborg A, Andersson J, Hunt PW, et al. Activation, exhaustion, and persistent decline of the antimicrobial MR1-restricted MAIT-cell population in chronic HIV-1 infection. Blood. 2013; 121: 1124-35.

[159]

Bohineust A, Tourret M, Derivry L, Caillat-Zucman S. Mucosal-associated invariant T (MAIT) cells, a new source of universal immune cells for chimeric antigen receptor (CAR)-cell therapy. Bull Cancer. 2021; 108: S92-5.

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