» Articles » PMID: 29334373

Prevention of Tuberculosis in Rhesus Macaques by a Cytomegalovirus-based Vaccine

Abstract

Despite widespread use of the bacille Calmette-Guérin (BCG) vaccine, tuberculosis (TB) remains a leading cause of global mortality from a single infectious agent (Mycobacterium tuberculosis or Mtb). Here, over two independent Mtb challenge studies, we demonstrate that subcutaneous vaccination of rhesus macaques (RMs) with rhesus cytomegalovirus vectors encoding Mtb antigen inserts (hereafter referred to as RhCMV/TB)-which elicit and maintain highly effector-differentiated, circulating and tissue-resident Mtb-specific CD4 and CD8 memory T cell responses-can reduce the overall (pulmonary and extrapulmonary) extent of Mtb infection and disease by 68%, as compared to that in unvaccinated controls, after intrabronchial challenge with the Erdman strain of Mtb at ∼1 year after the first vaccination. Fourteen of 34 RhCMV/TB-vaccinated RMs (41%) across both studies showed no TB disease by computed tomography scans or at necropsy after challenge (as compared to 0 of 17 unvaccinated controls), and ten of these RMs were Mtb-culture-negative for all tissues, an exceptional long-term vaccine effect in the RM challenge model with the Erdman strain of Mtb. These results suggest that complete vaccine-mediated immune control of highly pathogenic Mtb is possible if immune effector responses can intercept Mtb infection at its earliest stages.

Citing Articles

Systematic review of innate immune responses against complex infection in animal models.

Nieto Ramirez L, Mehaffy C, Dobos K Front Immunol. 2025; 15:1467016.

PMID: 39949719 PMC: 11821578. DOI: 10.3389/fimmu.2024.1467016.


Exploitation of Unconventional CD8 T-Cell Responses Induced by Engineered Cytomegaloviruses for the Development of an HIV-1 Vaccine.

Bruton J, Hanke T Vaccines (Basel). 2025; 13(1).

PMID: 39852851 PMC: 11769474. DOI: 10.3390/vaccines13010072.


HLA-E/ specific CD4 and CD8 T cells have a memory phenotype in individuals with TB infection.

Voogd L, Riou C, Scriba T, van Wolfswinkel M, van Meijgaarden K, Franken K Front Immunol. 2025; 15():1505329.

PMID: 39790998 PMC: 11714851. DOI: 10.3389/fimmu.2024.1505329.


Backtranslation of human RNA biosignatures of tuberculosis disease risk into the preclinical pipeline is condition dependent.

Painter H, Larsen S, Williams B, Abdelaal H, Baldwin S, Fletcher H mSphere. 2024; 10(1):e0086424.

PMID: 39651886 PMC: 11774039. DOI: 10.1128/msphere.00864-24.


Proceedings of the Conference "CMV Vaccine Development-How Close Are We?" (27-28 September 2023).

Schleiss M, Crooks C, Karthigeyan K, Kruc R, Otero C, Wang H Vaccines (Basel). 2024; 12(11).

PMID: 39591134 PMC: 11598149. DOI: 10.3390/vaccines12111231.


References
1.
Hansen S, Ford J, Lewis M, Ventura A, Hughes C, Coyne-Johnson L . Profound early control of highly pathogenic SIV by an effector memory T-cell vaccine. Nature. 2011; 473(7348):523-7. PMC: 3102768. DOI: 10.1038/nature10003. View

2.
Tameris M, Geldenhuys H, Luabeya A, Smit E, Hughes J, Vermaak S . The candidate TB vaccine, MVA85A, induces highly durable Th1 responses. PLoS One. 2014; 9(2):e87340. PMC: 3911992. DOI: 10.1371/journal.pone.0087340. View

3.
Griffiths K, Ahmed M, Das S, Gopal R, Horne W, Connell T . Targeting dendritic cells to accelerate T-cell activation overcomes a bottleneck in tuberculosis vaccine efficacy. Nat Commun. 2016; 7:13894. PMC: 5192216. DOI: 10.1038/ncomms13894. View

4.
Mattila J, Maiello P, Sun T, Via L, Flynn J . Granzyme B-expressing neutrophils correlate with bacterial load in granulomas from Mycobacterium tuberculosis-infected cynomolgus macaques. Cell Microbiol. 2015; 17(8):1085-97. PMC: 4570831. DOI: 10.1111/cmi.12428. View

5.
Fabregat A, Sidiropoulos K, Garapati P, Gillespie M, Hausmann K, Haw R . The Reactome pathway Knowledgebase. Nucleic Acids Res. 2015; 44(D1):D481-7. PMC: 4702931. DOI: 10.1093/nar/gkv1351. View