Vaccination Administration Considerations for Specific Populations

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  • Bavarian Nordic, manufacturer of JYNNEOS, has told the U.S. government it plans to put the vaccine on the commercial market around April 1, 2024.
  • Federal agencies are working with Bavarian Nordic to ensure that people will continue to have broad access to this vaccine, including people who are uninsured and underinsured. HHS Mpox Vaccine Operational Planning Guide
  • Mpox vaccination webpages are being updated to reflect commercialization of JYNNEOS.

Table 6. JYNNEOS and ACAM2000 Vaccination Administration Considerations for Specific Populations

Specific Population

Specific Population

Specific Population

JYNNEOS

JYNNEOS

JYNNEOS

ACAM2000

ACAM2000

ACAM2000

Administer 0.5mL subcutaneously, if vaccine is given.

Prior to administration in people younger than 6 months, clinicians should first contact their jurisdictional health department (Jurisdictional Contacts). Jurisdictional health departments can facilitate consultation with CDC if needed.

JYNNEOS

Administer 0.5mL subcutaneously, if vaccine is given.

Prior to administration in people younger than 6 months, clinicians should first contact their jurisdictional health department (Jurisdictional Contacts). Jurisdictional health departments can facilitate consultation with CDC if needed.

Do not administer to infants age <12 months.

ACAM2000

Do not administer to infants age <12 months.

People of any age who have a history of developing keloid scars

Specific Population

People of any age who have a history of developing keloid scars

Administer 0.5mL subcutaneously.

JYNNEOS

Administer 0.5mL subcutaneously.

Do not administer.

ACAM2000

Do not administer.

Most adults age ≥18 years who are eligible for vaccination under the national mpox vaccine strategy (includes PEP, PEP++, or PrEP)

Specific Population

Most adults age ≥18 years who are eligible for vaccination under the national mpox vaccine strategy (includes PEP, PEP++, or PrEP)

Administer 0.1mL intradermally or 0.5mL subcutaneously1.

JYNNEOS

Administer 0.1mL intradermally or 0.5mL subcutaneously1.

Administer percutaneously if vaccine is given.

ACAM2000

Administer percutaneously if vaccine is given.

People with prior history of smallpox vaccination2

Specific Population

People with prior history of smallpox vaccination2

Administer 0.1mL intradermally or 0.5mL subcutaneously1.

JYNNEOS

Administer 0.1mL intradermally or 0.5mL subcutaneously1.

Can be administered if no contraindication is present.

ACAM2000

Can be administered if no contraindication is present.

Administer 0.1mL intradermally or 0.5mL subcutaneously1.

JYNNEOS

Administer 0.1mL intradermally or 0.5mL subcutaneously1.

Do not administer.

ACAM2000

Do not administer.

People with three or more major cardiac risk factors5

Specific Population

People with three or more major cardiac risk factors5

Administer 0.1mL intradermally or 0.5mL subcutaneously1.

JYNNEOS

Administer 0.1mL intradermally or 0.5mL subcutaneously1.

Do not administer.

ACAM2000

Do not administer.

People with atopic dermatitis, eczema, or other exfoliative skin conditions6

Specific Population

People with atopic dermatitis, eczema, or other exfoliative skin conditions6

Administer 0.1mL intradermally or 0.5mL subcutaneously1.

JYNNEOS

Administer 0.1mL intradermally or 0.5mL subcutaneously1.

Do not administer.

ACAM2000

Do not administer.

People with prior history of mpox7

Specific Population

People with prior history of mpox7

See footnote about exceptions to the two-dose series.

JYNNEOS

See footnote about exceptions to the two-dose series.

Do not administer.

ACAM2000

Do not administer.

People with congenital or acquired immune deficiency disorders, including those taking immunosuppressive medications and people living with HIV (regardless of immune status)

Specific Population

People with congenital or acquired immune deficiency disorders, including those taking immunosuppressive medications and people living with HIV (regardless of immune status)

Administer as indicated based on age and history of keloids.

(Table 2)

JYNNEOS

Administer as indicated based on age and history of keloids.

(Table 2)

Do not administer.

ACAM2000

Do not administer.

1The JYNNEOS vaccine may be administered subcutaneously using the standard regimen or by using the alternative regimen (intradermal route). The patient and provider may discuss whether to administer the vaccine intradermally or subcutaneously.

2 Previous smallpox vaccination probably does provide some protection, but it may not necessarily be lifelong. During the 2003 mpox outbreak and during the current outbreak, several people who were infected with mpox had previously been vaccinated against smallpox decades prior. In response to the current outbreak, vaccines and other medical measures should be given to eligible people who were previously vaccinated against smallpox.

3 While there are no data for people who are pregnant, animal data do not show evidence of reproductive harm; pregnancy is not a contraindication to receiving JYNNEOS.

4 While there are no data for people who are breastfeeding, animal data do not show evidence of reproductive harm; breastfeeding is not a contraindication to receiving JYNNEOS. It is not known whether JYNNEOS is excreted in human milk. Data are not available to assess the impact of JYNNEOS on milk production or the safety of JYNNEOS in breastfed infants. However, because JYNNEOS vaccine is replication-deficient, it likely does not present a risk of transmission to breastfed infants and can be administered to women who are breastfeeding if vaccination is critical.

5 Presence of three or more of these major cardiac risk factors is a contraindication to vaccination with ACAM2000: hypertension, diabetes, hypercholesterolemia, heart disease at age ≤50 years in a first-degree relative, or smoking. Clinical studies have not detected an increased risk for myopericarditis in recipients of JYNNEOS. However, people with underlying heart disease (e.g., previous myocardial infarction, angina, congestive heart failure, cardiomyopathy, stroke or transient ischemic attack, or other heart conditions) or three or more major cardiac risk factors should be counseled about the theoretical risk for myopericarditis following vaccination with JYNNEOS given the uncertain etiology of myopericarditis associated with replication-competent smallpox vaccines such as ACAM2000.

6 Studies evaluating JYNNEOS in people with atopic dermatitis have demonstrated immunogenicity in eliciting a neutralizing antibody response. No concerning safety signals were revealed.

7 In the context of the current mpox outbreak, and while the supply of JYNNEOS vaccine is limited, the following are exceptions to the recommended two-dose series:

  • A person who is diagnosed with mpox after their first dose of JYNNEOS is not recommended to receive the second dose at this time, because mpox infection likely confers additional immune protection.
  • A person who would be eligible for vaccination but has been diagnosed with mpox during this outbreak, which started in the United States on May 17, 2022, is not recommended to be vaccinated at this time, because mpox infection likely confers immune protection.