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File: 102596_sep96_decls2_0001.txt
Subject: TRI SERVICE VACCINE TASK FORCE 7 DEC 90
Unit: OTSG
Parent Organization: HSC
Box ID: BX003202
Folder Title: DESERT SHIELD MEDICAL ISSUES REVIEW AND AD HOC WORKING GROUP
Document Number: 3
Folder SEQ #: 31
UNCLASSIFIED
DEPARTMENT OF THE ARMY
WALTER FTEED ARMY INSTFTUTE OF RE@CH
WALTER AEED ARA(Y #AEWAL CENTER
WASHINGTON. D.C. @-SIW
M FW-PLY AEFER Ta.
SGRD-UWZ-H 7 December 1990
MEMORANDUM THRU Commander, USA Medical Research and Development
Command, Fort Detrick, Frederick, Maryland
21701-5012
FOR The Surgeon General, 5109 Leesburg Pike, Falls Church, VA
22041-3258
SUBJECT: Tri-Service Vaccine Task Force (Appendix A)
BACKGROUND:
1. Diarrheal diseases have always been significant military
problems in Middle East campaigns (e.g. WWI, Gallipoli; WWII, El
Alamein; Suez crisis, UK, 1956; Lebanon, USA, 1957 and 1983;
Israeli Defense Force, 1966, 1972, 1983) and have been implicated
as cont-ribilitina determinants of victory (Rats, Lice and History,
H. Zinsser, c i939 Little-Brown, Co. Boston, MA). Diarrheal
diseases have already proven problematic in Desert Shield and
with the increasing likelihood of a continued U.S. presence, are
destined to become an even greater problem (Appendix B).
Furthermore, resistance to ciprofloxacin, the only currently
effective antibiotic to treat shigellosis, is predicted to occur
within 12-16 months (Appendix B).
2. Hepatitis A is transmitted by the fecal-oral route and
follows the same epidemiologic pattern as diarrheal diseases.
Hepatitis A was a significant problem for U.S. troops in the
North African campaign in WWII and is a persistent problem for
the Israeli Defense Force. Hence, our policy of prophylaxis with
Immune Serum Globulin. However, this requires repeated
ery three months and is an inadequate long termi
strategy (Appendix C).
3. Post wounding sepsis in modern warfare has become a major
cause of morbidity, mortality and cost. Hence, a USAMRDC mission
has been to develop vaccines against the major causes of post
wounding sepsis. Because of the difficulty in performing the
appropriate human studies, the approach taken has been to first
demonstrate efficacy by producing hyperimmune antisera and human
monoclonal antibodies and then fashion the antigen into a
vaccine. The individual vaccines are in various stages of
development (Appendix D).
EDMUND C. TRAMONT, COL, MC
Declassified per SECARMY by CMH: 10-1 5-1996
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Document 8 f:/Week-36/BX003202/DESERT SHIELD MEDICAL ISSUES REVIEW AND AD HOC WORKING GROUP/tri service vaccine task force 7 dec 90:1018961354253
Control Fields 17
File Room = sep96_declassified
File Cabinet = Week-36
Box ID = BX003202
Unit = OTSG
Parent Organization = HSC
Folder Title = DESERT SHIELD MEDICAL ISSUES REVIEW AND AD HOC WORKING GROUP
Folder Seq # = 31
Subject = TRI SERVICE VACCINE TASK FORCE 7 DEC 90
Document Seq # = 3
Document Date =
Scan Date =
Queued for Declassification = 01-JAN-1980
Short Term Referral = 01-JAN-1980
Long Term Referral = 01-JAN-1980
Permanent Referral = 01-JAN-1980
Non-Health Related Document = 01-JAN-1980
Declassified = 18-OCT-1996