This study is being conducted to collect safety and immunogenicity data for the WEE vaccine,
TSI-GSD 210. Enrollment in this protocol is offered for personnel who enter areas where this
virus is used in research or is endemic (an area where this disease process is found to occur
1. Be 18 to 65 years old at time of consent.
2. Have WEE plaque reduction neutralization 80% titers (PRNT80) < 1:10 for primary
3. Have WEE PRNT80 < 1:40 for booster series.
4. If female of childbearing potential, must agree to have a urine pregnancy test on the
same day before each vaccine. (Exception: documented hysterectomy or ≥ 3 years of
menopause.) The results must be negative. Females must agree to not become pregnant
for 3 months after receipt of the last study treatment (vaccination).
5. Be considered at risk for exposure to WEE virus and who have submitted a Request for
IND Vaccines for the WEE vaccine.
6. Sign and date the approved informed consent document and HIPAA Authorization.
7. Have in their charts
1. medical history (including concomitant medications) within 60 days of planned
first administration of vaccine
2. physical examination and laboratory tests within 1 year
3. previous chest radiograph and electrocardiogram
8. Be medically cleared for participation by an investigator. (Examinations and/or tests
may be repeated at the discretion of the enrolling physician.)
9. Be willing to return for all follow-up visits.
10. Agree to report any adverse events (AEs) that may or may not be associated with
administration of the vaccine for at least 28 days after administration and agree to
report all serious adverse events (for example, resulting in hospitalization) for the
duration of the subject's participation in the study.
11. Agree to defer blood, bone marrow, and organ donation for 1 year after receipt of the
1. Have completed previous WEE vaccine study as a nonresponder (PRNT80 < 1:40).
2. Have clinically significant abnormal laboratory results (including evidence of
hepatitis C, hepatitis B carrier state) or elevated liver function tests (two times
the normal range or at the discretion of the PI).
3. Have a personal history of an immunodeficiency or received treatment with an
immunosuppressive medication, such as systemically administered glucocorticoids (eg,
prednisone) within 1 month before planned administration of the vaccine or with other
immunosuppressive therapies within 6 months of planned administration of the vaccine.
Other immunosuppressive therapies include all cancer chemotherapeutic agents, drugs to
prevent transplant rejection, interferons, monoclonal antibodies, protein kinase
inhibitors, methotrexate, TNF (tumor necrosis factor) inhibitors, and any other drug
determined to be immunosuppressive by the PI. Current administration of topical,
inhalational, or intranasal glucocorticoids is not excluded.
4. Have a confirmed HIV infection (antibody positivity).
5. Have a positive pregnancy test or be a breastfeeding female.
6. Have any known allergies to components of the vaccine:
formaldehyde eggs neomycin sulfate human serum albumin sodium bisulfite
7. Have administration of another vaccine or investigational product within 28 days of
8. Have any unresolved AE resulting from a previous immunization.
9. A medical condition that, in the judgment of the PI, would impact subject safety.