Table 6.
Vaccine | Recommended for use after HCT | Time post-HCT to initiate vaccine | Number of dosesa | Improved by donor vaccination (practicable only in related-donor setting) |
---|---|---|---|---|
Pneumococcal Conjugate (PCV) | Yes (BI) | 3–6 mo | 3–4b | Yes; may be considered when the recipient is at high risk for chronic GVHD |
Tetanus, diphtheria, acellular pertussisc | Yes Tetanus-diphtheria: (BII) Pertussis (CIII) |
6–12 mo | 3d | Tetanus: likely Diphtheria: likely Pertussis: unknown |
Haemophilus influenzae conjugate | Yes (BII) | 6–12 mo | 3 | Yes |
Meningococcal conjugate | Follow country recommendations for general population (BII) | 6–12 mo | 1 | Unknown |
Inactivated Polio | Yes (BII) | 6–12 mo | 3 | Unknown |
Recombinant Hepatitis B | Follow country recommendations for general population (BII) | 6–12 mo | 3 | Likelye |
Inactivated Influenza | Yearly (AII) | 4–6 mo | 1 –2f | Unknown |
Measles-Mumps-Rubellag (live) | Measles: All children and seronegative adults Measles:BII Mumps:CIII Rubella:BIII EIII (<24 mo post HCT, active GVHD, on immune suppression) |
24 mo | 1 –2h | Unknown |
Notes:
A uniform specific interval between doses cannot be recommended as various intervals have been used in studies. As a general guideline, a minimum of 1 month between doses may be reasonable.
Following the primary series of 3 PCV doses, a dose of the 23-valent polysaccharide pneumococcal vaccine (PPSV23) to broaden the immune response might be given (BII). For patients with chronic GVHD who are likely to respond poorly to PPSV23, a fourth dose of the PCV should be considered instead of PPSV23 (CIII).
DTaP is preferred, however, if only Tdap is available (eg, because TDaP is not licensed for adults), administer Tdap. Acellular pertussis vaccine is preferred, but the whole-cell pertussis vaccine should be used if it is the only pertussis vaccine available. (See text for more information)
See text for consideration of an additional dose(s) of tetanus toxoid–reduced diphtheria toxoid–reduced acellular pertussis vaccine (Tdap) for older children and adults
Significant improvement of recipient response to hepatitis B vaccine posttransplant can be expected only if the donor receives more than 1 hepatitis vaccine dose prior to donation.
For children < 9 years of age, 2 doses are recommended yearly between transplant and 9 years of age. [306].
Measles, mumps, and rubella vaccines are usually given together as a combination vaccine. In females with pregnancy potential, vaccination with rubella vaccine either as a single or a combination vaccine is indicated.
In children, 2 doses are favored.