Piloting delivery of PfSPZ vaccines for malaria through a cryogenic vaccine cold chain to travel and military medicine clinics

Author:

James Eric R1,Church L W Preston1,Hoffman Stephen L1,Richie Thomas L1,Robertson Brian D2,Hickey Patrick W3,Schwartz David J2,Logan Patrick T2,Asare Theresa D2,Jones Macie L2,Bay Jeannie L4,Roschel Austin K4,Pfeiffer Jacqueline L4,Acosta Rebecca W5,Schiavi Ethan5,Acosta Alberto M5,Noble Mark6,Henkel Thomas6,Young Cebrina6

Affiliation:

1. Sanaria Inc , Rockville, MD 20850 , USA

2. Walter Reed National Military Medical Center , Bethesda, MD 20889 , USA

3. Uniformed Services University of the Health Sciences , Bethesda, MD 20814 , USA

4. Joint Base Lewis-McChord/Madigan Army Medical Center , Lewis-McChord, WA 98431 , USA

5. Traveler’s Medical Service , New York, NY 10022 , USA

6. Passport Health Silver Spring Travel Clinic , Silver Spring, MD 20903 , USA

Abstract

Abstract Background PfSPZ vaccines comprising Plasmodium falciparum (Pf) sporozoites (SPZ) have demonstrated > 90% protection against variant Pf malaria infections for at least 12 weeks; they are the only vaccines with the level of efficacy necessary to protect travellers. PfSPZ are eukaryotic cells stabilized by cryopreservation and distributed using a cryogenic (below −150 °C) cold chain. The Ebola vaccine and mRNA vaccines against SARS-CoV-2 pioneered uptake of vaccines requiring non-standard ultra-low temperature cold chains. The cryogenic cold chain using liquid nitrogen (LN2) vapour phase (LNVP) cryoshippers, is simpler, more efficient than −80, −20 or 2–8 °C cold chains, and does not use electricity. This study was conducted to evaluate implementation and integration of a cryogenically distributed vaccine at travel and military immunization clinics. Methods We conducted sequential 28-day studies evaluating vaccine shipping, storage, maintenance and accession at two US military and two civilian travel health/immunization clinics. In each clinic, personnel were trained in equipment use, procurement and handling of LN2, temperature monitoring and inventory record keeping by in-person or video instruction. Results Sites required 2–4 h/person for two persons to assimilate and develop the expertise to manage vaccine storage and LNVP operations. LN2 for recharging cryoshippers was delivered every 1–2 weeks. Vaccine ordering, receipt, storage and inventory control was conducted effectively. Simulated single dose vaccine cryovial retrieval and thawing were performed successfully in different travel clinic settings. Continuous temperature monitoring at each site was maintained with only one short excursion above −150 °C (−145 °C) through shipping, use and reverse logistics. Staff, during and at study conclusion, provided feedback that has been incorporated into our models for cold chain logistics. Conclusions These studies demonstrated that the training in delivery, storage, administration and integration of PfSPZ vaccines can be successfully managed in different immunization clinic settings for travellers and military personnel.

Funder

National Institute of Allergy and Infectious Diseases

National Institutes of Health

Department of Defense

Publisher

Oxford University Press (OUP)

Subject

General Medicine

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