Laboratory Testing for Vaccinia and Related Differential Diagnoses

General
Clinical materials suspected of containing vaccinia should be forwarded to an appropriate laboratory in the CDC-sponsored Laboratory Response Network (LRN) for evaluation. Such laboratories have standardized protocols for assessment of such samples and vaccinated staff who can perform these studies. LRN laboratories include local and state public health laboratories with special security and bio-containment capability. Consult your local and state health departments for the closest LRN laboratory with vaccinia capability.

Diagnostic Tests
We recommend that expert consultation with the CDC be undertaken in serious complications to obtain the best advice as to diagnosis in specific situations.

In most instances, differentiation of an adverse event after vaccination from other infectious or non-infectious diseases must be accomplished. In those cases the appropriate diagnostic tests for the alternative diseases, such as chickenpox, should be employed simultaneously with tests for vaccinia virus. A comprehensive algorithm has been developed by CDC for the evaluation of rash illness suspected to be poxvirus in origin.

Laboratory diagnosis of infectious complications consists of rapid diagnostic tests and traditional culture techniques. Tests for varicella include special stains of smears of lesions, direct and indirect immunofluorescent methods, the polymerase chain reaction and culture. Electron microscopy of lesion material can be useful in differentiating herpesviruses from poxviruses such as vaccinia, but a limited number of centers have this capability. Vaccinia can be readily grown in routine cell culture and definitively identified by referral to a specialty laboratory in the LRN and/or CDC. A polymerase chain reaction assay configured to detect vaccinia is under evaluation for deployment to the LRN.

In all instances the LRN laboratory should be consulted immediately to determine the appropriate test for the clinical circumstances and the correct method for collection of specimens and transport to the laboratory.

Immunologic studies are suggested for serious complications to better understand the pathogenesis of adverse events. Tests for the presence of HIV antibody and flow cytometry to determine degree of immunodeficiency in HIV-positives is indicated. Workup for hematologic malignancy or lymphoma may be appropriate.