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The Australian Immunisation Handbook 10th Edition 2013

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3.3.3 Vaccination of immunocompromised persons<br />

A person can be immunocompromised due to disease and/or medical<br />

treatment. Vaccination of immunocompromised persons presents numerous<br />

challenges. <strong>The</strong> immune protection attained from previous immunisation<br />

may be diminished; the response to vaccines administered in the setting of<br />

immunocompromise may be reduced, with additional booster vaccine doses<br />

required; the risk of vaccine-preventable diseases and/or their complications<br />

may be increased; and the risk of adverse events from live vaccines may be<br />

increased. Degrees of immunocompromise vary from insignificant to profound,<br />

and this, together with the risk of acquiring vaccine-preventable disease, should<br />

be taken into account when considering a vaccination schedule.<br />

When considering vaccination of persons on immunosuppressive therapy, it is<br />

particularly important to consider a number of factors, including the biologic<br />

target of the medication being used (mechanism and duration of effect on the<br />

immune system) as well as the consequence of using combination therapies<br />

(e.g. prednisolone and methotrexate), which can contribute to the nature,<br />

extent and length of immunocompromise. It is also important to know the<br />

anticipated duration of immunocompromise, whether due to therapy or the<br />

underlying disease (see also ‘Immunocompromise associated with corticosteroid<br />

administration’ below). In some instances, additional booster doses of vaccines<br />

may be required to optimise protection in immunocompromised persons<br />

(e.g. pneumococcal vaccines at diagnosis of haematological malignancy).<br />

To determine the need for booster doses, it may be useful to measure postvaccination<br />

antibody titres in selected groups in some circumstances, such as<br />

for adults or children who have received haematopoietic stem cell transplants<br />

(see ‘Haematopoietic stem cell transplant recipients’ below). Reliable serological<br />

testing is not readily available and/or validated to measure vaccine-induced<br />

immunity for all vaccines, and, in addition, results should be interpreted using<br />

standardised serological correlates. (See also 2.1.5 Catch-up, ‘Use of serological<br />

testing to guide catch-up vaccination’.) Expert advice should be sought if<br />

required.<br />

Many vaccine-preventable diseases are associated with an increased risk of<br />

morbidity and mortality in immunocompromised persons. Two important<br />

examples are influenza and invasive pneumococcal disease (IPD). Annual<br />

influenza vaccination should be given to all immunocompromised persons<br />

≥6 months of age (see 4.7 Influenza). Immunocompromised persons may<br />

also require additional doses of pneumococcal vaccines; the timing, number<br />

of doses and type of vaccine(s) vary depending on age and the underlying<br />

risk for IPD (see 4.13 Pneumococcal disease). <strong>The</strong>se, and other specific vaccine<br />

recommendations, are discussed in more detail below.<br />

All immunocompromised persons, irrespective of age, who receive influenza<br />

vaccine for the first time are recommended to receive 2 vaccine doses, at least<br />

4 weeks apart, and 1 dose annually thereafter (see 4.7 Influenza). Where it is<br />

PART 3 VACCINATION FOR SPECIAL RISK GROUPS 145<br />

3.3 GROUPS WITH SPECIAL<br />

VACCINATION REQUIREMENTS

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