Peter F. Billingsley

ORCID: 0000-0003-1142-4813
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About
Contact & Profiles
Research Areas
  • Mosquito-borne diseases and control
  • Malaria Research and Control
  • Insect Resistance and Genetics
  • Invertebrate Immune Response Mechanisms
  • Insect symbiosis and bacterial influences
  • Parasites and Host Interactions
  • Vector-borne infectious diseases
  • Travel-related health issues
  • Trypanosoma species research and implications
  • Viral Infectious Diseases and Gene Expression in Insects
  • Insect Pest Control Strategies
  • Complement system in diseases
  • Insect-Plant Interactions and Control
  • Neurobiology and Insect Physiology Research
  • HIV Research and Treatment
  • Research on Leishmaniasis Studies
  • Helminth infection and control
  • Hepatitis B Virus Studies
  • Parasite Biology and Host Interactions
  • vaccines and immunoinformatics approaches
  • Insect Utilization and Effects
  • Viral Infections and Vectors
  • Vector-Borne Animal Diseases
  • Insect behavior and control techniques
  • Study of Mite Species

Sanaria
2016-2025

Narrative (Sweden)
2025

University of Maryland, Baltimore
2010-2015

Protein Potential (United States)
2010-2015

Emmes (United States)
2015

Centers for Disease Control and Prevention
2015

Howard Hughes Medical Institute
2015

University of Aberdeen
1999-2013

Imperial College London
1988-2010

Radboud University Nijmegen
2010

Robert A. Seder Lee-Jah Chang Mary E. Enama Kathryn L. Zephir Uzma Sarwar and 95 more Ingelise J. Gordon LaSonji A. Holman Eric R. James Peter F. Billingsley Anusha Gunasekera Adam Richman Sumana Chakravarty Anita Manoj Vel Murugan MingLin Li Adam J. Ruben Li Tao Abraham G. Eappen R. E. Stafford Sarah Plummer Cynthia S. Hendel Laura Novik Pamela Costner Floreliz Mendoza Jamie Saunders Martha Nason Jason H. Richardson Jittawadee Murphy Silas A. Davidson Thomas L. Richie Martha Sedegah Awalludin Sutamihardja Gary A. Fahle Kirsten E. Lyke Matthew B. Laurens Mario Roederer Kavita Tewari Judith E. Epstein B. Kim Lee Sim Julie E. Ledgerwood Barney S. Graham Stephen L. Hoffman Cassandra DiGiovanni Pernell Williams Nicole Luongo Jillian Mitchell Maria Burgos Florez Brenda Larkin Nina M. Berkowitz Brandon Wilson Tanya Clarke Olga Vasilenko Galina V. Yamshchikov Sandra Sitar LaChonne Stanford Iris Pittman Robert T. Bailer Joseph P. Casazza Hope DeCederfelt Judith Starling Esther C. Williams Anna F. Lau Stella Antonara Jeffery Brocious Margaret A. Kemp James Inglese Patricia Dranchak Esteban Abot Sharina Reyes Harini Ganeshan María Belmonte Jun Huang Arnel Belmonte Jack Komisar Yonas Abebe Yeab Getachew Asha Patil Steve Matheny K. E. Nelson James Overby Virak Pich Yingda Wen Richard Fan Enni Fomumbod Aderonke Awe Chinnamma Chakiath Mary D. King Maria Socorro Orozco Tooba Murshedkar Debbie Padilla Bing Jiang Lixin Gao Natasha KC Rui Xu Matthew Adams Christopher V. Plowe Hayley Loblein Phyllis Renehan Meghan Kunchai Ly Diep

Consistent, high-level, vaccine-induced protection against human malaria has only been achieved by inoculation of Plasmodium falciparum (Pf) sporozoites (SPZ) mosquito bites. We report that the PfSPZ Vaccine--composed attenuated, aseptic, purified, cryopreserved PfSPZ--was safe and well tolerated when administered four to six times intravenously (IV) 40 adults. Zero subjects receiving five doses three nine 1.35 × 10(5) Vaccine nonvaccinated controls developed after controlled infection (P =...

10.1126/science.1241800 article EN Science 2013-08-09

Our goal is to develop a vaccine that sustainably prevents Plasmodium falciparum (Pf) malaria in ≥80% of recipients. Pf sporozoites (PfSPZ) administered by mosquito bites are the only immunogens shown induce such protection humans. Such thought be mediated CD8(+) T cells liver secrete interferon-γ (IFN-γ). We report purified irradiated PfSPZ 80 volunteers needle inoculation skin was safe, but suboptimally immunogenic and protective. Animal studies demonstrated intravenous immunization...

10.1126/science.1211548 article EN Science 2011-09-09

Significance A highly effective malaria vaccine capable of long-term protection against genetically diverse strains is urgently needed. Here, we demonstrate that a three-dose regimen live attenuated whole-parasite conferred durable sterile through 33 weeks in ∼50% subjects controlled human infection strain heterologous to the strain. Prior studies by others and us have shown T cells are critical mediating after live-attenuated vaccination. provide evidence this Plasmodium falciparum...

10.1073/pnas.1615324114 article EN Proceedings of the National Academy of Sciences 2017-02-21

BACKGROUND: A radiation-attenuated Plasmodium falciparum (Pf) sporozoite (SPZ) malaria vaccine, PfSPZ Vaccine, protected 6 of subjects (100%) against homologous Pf (same strain as in the vaccine) controlled human infection (CHMI) 3 weeks after 5 doses administered intravenously. The next step was to assess protective efficacy heterologous (different from vaccine), fewer doses, and at 24 weeks. METHODS: trial assessed tolerability, safety, immunogenicity, direct venous inoculation (DVI) or...

10.1172/jci.insight.89154 article EN JCI Insight 2017-01-11

With a growing world population and increasingly demanding consumers, the production of sufficient protein from livestock, poultry, fish represents serious challenge for future. Approximately 1,900 insect species are eaten worldwide, mainly in ...Read More

10.1146/annurev.en.35.010190.001251 article EN Annual Review of Entomology 1990-01-01

Controlled human malaria infection with sporozoites is a standardized and powerful tool for evaluation of vaccine drug efficacy but so far only applied by exposure to bites Plasmodium falciparum (Pf)-infected mosquitoes. We assessed in an open label Phase 1 trial, after intradermal injection respectively 2,500, 10,000, or 25,000 aseptic, purified, vialed, cryopreserved Pf (PfSPZ) three groups ( N = 6/group) healthy Dutch volunteers. Infection was safe parasitemia developed 15 18 volunteers...

10.4269/ajtmh.2012.12-0613 article EN other-oa American Journal of Tropical Medicine and Hygiene 2012-11-14

We are using controlled human malaria infection (CHMI) by direct venous inoculation (DVI) of cryopreserved, infectious Plasmodium falciparum (Pf) sporozoites (SPZ) (PfSPZ Challenge) to try reduce time and costs developing PfSPZ Vaccine prevent in Africa. Immunization with five doses at 0, 4, 8, 12, 20 weeks 2.7 × 105 gave 65% vaccine efficacy (VE) 24 against mosquito bite CHMI U.S. adults 52% (time event) or 29% (proportional) VE over naturally transmitted Pf Malian adults. assessed the...

10.4269/ajtmh.17-1014 article EN cc-by American Journal of Tropical Medicine and Hygiene 2018-06-26

Controlled human malaria infection (CHMI) by mosquito bite has been used to assess anti-malaria interventions in > 1,500 volunteers since development of methods for infecting mosquitoes feeding on Plasmodium falciparum (Pf) gametocyte cultures. Such CHMIs have never Africa. Aseptic, purified, cryopreserved Pf sporozoites, PfSPZ Challenge, were infect Dutch intradermal injection. We conducted a double-blind, placebo-controlled trial safety and infectivity Challenge adult male Tanzanians....

10.4269/ajtmh.14-0119 article EN cc-by American Journal of Tropical Medicine and Hygiene 2014-07-29

Controlled human malaria infection (CHMI) accelerates development of anti-malarial interventions. So far, CHMI is done by exposure volunteers to bites five mosquitoes carrying Plasmodium falciparum sporozoites (PfSPZ), a technique available in only few centres worldwide. Mosquito-mediated logistically complex, exact PfSPZ dosage impossible and live mosquito-based interventions are not suitable for further clinical development. An open-labelled, randomized, dose-finding study 18–45 year old,...

10.1186/s12936-015-0628-0 article EN cc-by Malaria Journal 2015-03-17

Mosquito fitness is determined largely by body size and nutritional reserves. Plasmodium infections in the mosquito resultant transmission of malaria parasites might be compromised vector's status. We studied effects stress parasite on Anopheles mosquitoes.Larvae gambiae sensu stricto An. stephensi were reared at constant density but with nutritionally low high diets. Fitness adult mosquitoes resulting from each dietary class was assessed measuring lipid, protein glycogen content. The first...

10.1186/1756-3305-6-345 article EN cc-by Parasites & Vectors 2013-12-01

Controlled human malaria infection (CHMI) studies are a vital tool to accelerate vaccine and drug development. As CHMI trials performed in controlled environment, they allow unprecedented, detailed evaluation of parasite growth dynamics (PGD) immunological responses. However, have not been routinely malaria-endemic countries or used investigate mechanisms naturally-acquired immunity (NAI) Plasmodium falciparum.We conducted an open-label, randomized pilot-study using aseptic, cryopreserved P....

10.3389/fmicb.2014.00686 article EN cc-by Frontiers in Microbiology 2014-12-12

In the context of stalling progress against malaria, resistance mosquitoes to insecticides, and residual transmission, mass drug administration (MDA) ivermectin, an endectocide used for neglected tropical diseases (NTDs), has emerged as a promising complementary vector control method. Ivermectin reduces life span

10.4269/ajtmh.19-0620 article EN American Journal of Tropical Medicine and Hygiene 2020-01-23

Background Controlled human malaria infection (CHMI) studies have become a routine tool to evaluate efficacy of candidate anti-malarial drugs and vaccines. To date, CHMI trials mostly been conducted using the bite infected mosquitoes, restricting number trial sites that can perform studies. Aseptic, cryopreserved P. falciparum sporozoites (PfSPZ Challenge) provide potentially more accurate, reproducible practical alternative, allowing known be administered simply by injection. Methodology We...

10.1371/journal.pone.0065960 article EN cc-by PLoS ONE 2013-06-18
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