Description

An HIV-infected patient started on highly active antiretroviral therapy (HAART) may transform from being immune deficient to more immunocompetent. Many patients are able to discontinue prophylaxis to opportunistic infections, while other patients may clinically react to previously occult infections.


Measure

Immune Deficient

Immune Restoration

absolute CD4 lymphocyte count

low

increase

response to vaccines

no antibody response

develops antibody response

response to delayed type hypersensitivity skin test

anergy

responsive

prophylactic therapy against opportunistic pathogens

needs

can discontinue

HIV viral loads

high

undetectable while on therapy

 

Immune Restoration Disease refers to clinical deterioration in patients as they become able to respond to occult infections. It tends to occur during the first 6 months of HAART therapy and may be associated with reactions to:

(1) Mycobacterium avium-intracellulare complex (lymphadenopathy, other)

(2) Cytomegalovirus (usually retinitis)

(3) Herpes zoster

(4) viral hepatitis B or C

(5) Mycobacterium tuberculosis

(6) Herpes simplex

(7) JC virus

(8) Cryptococcus neoformans

(9) Kaposi's sarcoma

 

Differential diagnosis:

(1) failure in drug regimen due to resistance (relapse of occult infection)

(2) new opportunistic infection associated with partially restored but defective immunity

(3) adverse drug reaction

 

For patients with immune restoration:

(1) corticosteroids may be beneficial

(2) HAART therapy should be continued (patients with viral hepatitis or Kaposi's sarcoma may benefit from holding therapy temporarily)

(3) if effective therapy is available for the underlying process, then this should be considered (antifungal, antimycobacterial, anti-CMV)

(4) analgesics

 


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