Available Vaccines
Mpox
Introduction
Mpox is caused by the monkeypox virus (MPXV), an enveloped double-stranded DNA virus. It is a member of the Orthopoxvirus genus in the family Poxviridae. There are two distinct clades of the virus: clade I (Central African/ Congo Basin) (subclades Ia and Ib) and clade II (West African) (subclades IIa and IIb). Clade I infections are generally more severe and more transmissible, with higher mortality rates, while Clade II infections are typically milder and were responsible for the 2022–2023 global outbreak and continues to circulate internationally.
Mpox can be transmitted through close contact with an individual who has mpox, with contaminated materials, or with infected animals. The virus can spread between people through skin-to-skin contact with sores, scabs, respiratory droplets or oral fluids, usually through close, intimate situations. Most of the recent spike in cases has been through sexual transmission. Infection is also transmitted through contact with animals, such as via infected rodents through broken skin (bites or scratches), or direct contact with an infected animal’s blood, bodily fluids or pox lesions (sores).
Incubation period is 5-13 days, although it can take up to 21 days. Early symptoms include fever, headache, muscle ache, backache, swollen lymph nodes, chills and exhaustion, followed by a rash on the face, hands and feet, that can spread to the inside of the mouth, the genitals and the cornea. The rash can last 2–4 weeks. With no specific antiviral treatment available, treatment of Mpox is mainly symptomatic.
Mpox was first discovered in 1958 when outbreaks of a disease that caused pox-like symptoms were discovered in monkeys held in captivity for research. It was first seen in humans in 1970 in the Democratic Republic of the Congo (DRC) and it is now endemic in Central and West Africa. The geographic range of mpox is mostly West and Central Africa.
In 2017, Nigeria saw a re-emergence of cases after nearly four decades of zero cases; and the disease was spreading in an unusual way. Most patients were young men who had lesions or skin rashes and ulcers around the genital area, which suggested that mpox might also be spread through sexual contact. By this point, DRC had also seen cases steadily rising. A global outbreak of clade IIb began in 2022 and continues to this day, including in some African countries. There are also growing outbreaks of clades Ia and Ib affecting the DRC and other countries in Africa. As of 2024, clade Ib has also been detected beyond Africa.
In May 2022, a case of mpox was detected in the UK, and soon several more, apparently unconnected cases, were found, spreading across borders in Europe and to the US. It soon emerged that most of the cases across Europe and the US were in men who have sex with men, especially those who had closely connected sexual networks, allowing the virus to spread in a different way than in the general population. By July 2022, WHO declared the global outbreak a Public Health Emergency of International Concern (PHEIC). The 2022–2023 global outbreak was caused by the clade IIb mpox strain
Just over a year later, on 14 August 2024, WHO declared once more that mpox was a PHEIC. This declaration was prompted by a surge of mpox cases in countries like DRC, and also in neighbouring countries that had never seen mpox before, such as Burundi, Kenya, Rwanda and Uganda. This was caused by the more deadly clade I strain.
In 2025, it was reported to WHO that between January–May 2025, 24,672 confirmed cases and 82 deaths were reported across 75 countries. Most cases were in Africa, especially Central and East Africa. Outside Africa, smaller clusters continue in Europe, North America, Asia, and Latin America, mostly linked to Clade II.
Vaccines
Vaccines are available for mpox and should be considered along with other public health interventions. The smallpox vaccine, which uses the vaccinia virus, is closely related to the mpox virus and provides partial cross-protection against mpox infection, although this immunity wanes over time. This connection has driven the development of vaccines specifically for mpox. The smallpox vaccine that can prevent about 85% of mpox cases have been deployed in recent emergencies to curb transmission. Available evidence shows mpox vaccines are safe and well tolerated in most people.
Table 19.1 Mpox Vaccines

In Malaysia, mpox vaccines are not part of a general public health programme. Malaysia received 2,220 doses of the JYNNEOS (MVA‑BN) vaccine in February 2025 through the ASEAN Covid‑19 Response Fund. The coverage is sufficient for about 1,100 individuals, since JYNNEOS requires two doses. The Ministry of Health is prioritizing frontline healthcare workers and close contacts of confirmed cases, using limited supplies of the JYNNEOS vaccine and reinforcing the ring‑vaccination approach. Vaccination is administered only after medical expert evaluation. Malaysia’s rollout mirrors a global strategy of limited doses, targeted use, and outbreak containment as opposed to broad public immunization.
Meanwhile, BioNTech, in partnership with CEPI (Coalition for Epidemic Preparedness Innovations) started a Phase 1/2 clinical trial of the mRNA-based mpox vaccine candidate, BNT166.
Implication for Health Care Workers (HCWs)
Targeted approach and priority groups for vaccination currently as above.
Evidence of Safety & Effectiveness
JYNNEOS has demonstrated strong safety and efficacy in clinical trials, with mild adverse effect such as injection site pain, fever, and fatigue. It has been shown to provide effective protection in populations at risk of infection. ACAM2000, while effective, has more serious adverse effects, including myocarditis, pericarditis, and severe skin reactions, which make it less ideal for immunocompromised individuals. Both vaccines appear to be highly effective in preventing severe disease, reducing viral transmission, and shortening the duration of illness when used in PEP or PrEP settings.
A 2015 clinical study evaluated a two-dose series of JYNNEOS given intradermally compared to subcutaneously in individuals ≥18 years old. Individuals who received the vaccine intradermally received a lower volume (one fifth) than individuals who received the vaccine subcutaneously. The results of this study demonstrated that intradermal administration produced a similar immune response to subcutaneous administration. Administration by the intradermal route resulted in more redness, firmness, itchiness and swelling at the injection site, but less pain.
References
- Bavarian Nordic. (March 2025). JYNNEOS vaccine. Prescribing Information. https://bavariannordic.io/uploads/jynneos-pi.pdf
- Esteban Ortiz-Prado, E., Kyriakidis, N. C., López-Cortés, A., et al. (2025). Current and emerging mpox vaccine strategies: A comprehensive review. Vaccine, 62, 127598. https://doi.org/10.1016/j.vaccine.2025.127598
- Grabenstein, J. D., & Hacker, A. (2024). Vaccines against mpox: MVA-BN and LC16m8. Expert Review of Vaccines, 386, e078243. https://doi.org/10.1080/14760584.2024.2397006
- Hraib, M., Jouni, S., Albitar, M.M., Alaidi, S., and Aishehabi, Z. (June 2022). The outbreak of monkeypox 2022: An overview. Ann Med Surg (Lond),79:104069. DOI: 1016/j.amsu.2022.104069
- Kennedy, J.S., Gurwith, M., Dekker, C.L., et al. (2011). Safety and immunogenicity of LC16m8: An attenuated smallpox vaccine in vaccinia-naive adults. Journal of Infectious Diseases, 204, 1395–1402. https://doi.org/10.1093/infdis/jir527
- Lauren, P., Martini, B.A., Yu, N., et al. (2024). Vaccine effectiveness of 3rd generation mpox vaccines against mpox and disease severity: A systematic review and meta-analysis. Vaccine, 42(25), 126053. https://doi.org/10.1016/j.vaccine.2024.06.021
- Ministry of Health Malaysia. (2025). Reten pemantauan dan pemberian vaksin Mpox (MVA-BN) di fasiliti. Bahagian Kawalan Penyakit, KKM.
- Nalca, A., & Zumbrun, E. E. (2010). ACAM2000: The new smallpox vaccine for the United States Strategic National Stockpile. Drug Design, Development and Therapy, 4, 71–79. https://doi.org/10.2147/dddt.s3687
- Navarro, C., Lau, C., Buchan, S. A., et al. (2024). Effectiveness of modified vaccinia Ankara-Bavarian Nordic vaccine against mpox infection: Emulation of a target trial. BMJ, 386. https://doi.org/10.1136/bmj-2023-078243
- Pittman, P. R., Hahn, M., Lee, H. S., et al. (2019). Phase 3 efficacy trial of modified vaccinia Ankara as a vaccine against smallpox. New England Journal of Medicine, 381, 1897–1908. DOI: 1056/NEJMoa1817307
- Rao, A.K., Peterson, B.W., Whitehill, F., et al. (2022). Use of JYNNEOS (Smallpox and Monkeypox Vaccine, Live, Nonreplicating) for Preexposure Vaccination of Persons at Risk for Occupational Exposure to Orthopoxviruses: Recommendations of the Advisory Committee on Immunization Practices — United States, 2022. MMWR,71(22):734-742. https://www.cdc.gov/mmwr/volumes/71/wr/pdfs/mm7122e1-H.pdf
- Shafaati, M., Forghani, S., Shahsavand Davoudi, A., et al. (2025). Current advances and challenges in mpox vaccine development: A global landscape. Therapeutic Advances in Vaccines and Immunotherapy, 13, 25151355251314339. https://doi.org/10.1177/25151355251314339
- Wang, X., Gu, Z., Sheng, S., Song, R., & Jin, R. (2024). The current state and progress of mpox vaccine research. China CDC Weekly, 6(7), 118–125. https://doi.org/10.46234/ccdcw2024.025
- World Health Organization. (August 2024). Mpox: Fact sheet. https://www.who.int/news-room/fact-sheets/detail/monkeypox
- World Health Organization. (April 22, 2025). LC16m8 (live-attenuated freeze-dried vaccinia) smallpox and mpox vaccine: Interim guidance. https://iris.who.int/server/api/core/bitstreams/9b10eb01-fbfd-4f9f-81b7-9c29ddbcc560/content
- Zhai, Y. Q., Han, Y. Z., Wang, W. L., & Tan, W. J. (2025). Advancements in mpox vaccine development: A comprehensive review of global progress and recent data. Biomedical and Environmental Sciences, 38(2), 248–254. https://doi.org/10.3967/bes2024.121