Physician
Infectious Disease
Dr. Peter D. Crompton, MD
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Doctor Peter D. Crompton, MD practices Infectious Disease. He went to medical school at Johns Hopkins University School of Medicine. Johns Hopkins University School of Medicine is one of the top medical schools in the US. Johns Hopkins University School of Medicine is ranked 3/29 in Research/PrimaryCare. Peter D. Crompton is also published. He has 27 publications published. The lastest publication: "Plasmodium falciparum Gametocyte-Specific Antibody Profiling Reveals Boosting through Natural Infection and Identifies Potential Markers of Gametocyte Exposure.' He is registered with Medicare and accepts Medicare payments.
Publications
- Plasmodium falciparum Gametocyte-Specific Antibody Profiling Reveals Boosting through Natural Infection and Identifies Potential Markers of Gametocyte Exposure.
- Novel serologic biomarkers provide accurate estimates of recent Plasmodium falciparum exposure for individuals and communities.
- RTS,S Vaccination Is Associated With Serologic Evidence of Decreased Exposure to Plasmodium falciparum Liver- and Blood-Stage Parasites.
- Gut Microbiota Elicits a Protective Immune Response against Malaria Transmission.
- Co-infection of Long-Term Carriers of Plasmodium falciparum with Schistosoma haematobium Enhances Protection from Febrile Malaria: A Prospective Cohort Study in Mali.
- Exposure-dependent control of malaria-induced inflammation in children.
- Naturally Acquired Antibodies Specific for Plasmodium falciparum RH5 Inhibit Parasite Growth and Predict Protection From Malaria.
- Young lives lost as B cells falter: what we are learning about antibody responses in malaria.
- An Intensive Longitudinal Cohort Study of Malian Children and Adults Reveals No Evidence of Acquired Immunity to Plasmodium falciparum Infection.
- Systems immunology of human malaria.
- Plasmodium falciparum malaria in the low transmission Peruvian Amazon is associated with immunologic memory.
- Therapeutic blockade of PD-L1 and LAG-3 rapidly clears established blood-stage Plasmodium infection.
- Hemoglobin S and C Heterozygosity Enhances Neither the Magnitude nor Breadth of Antibody Responses to a Diverse Array of Plasmodium falciparum Antigens.
- High efficiency human memory B cell assay and its application to studying Plasmodium falciparum-specific memory B cells in natural infections.
- A positive correlation between atypical memory B cells and Plasmodium falciparum transmission intensity in cross-sectional studies in Peru and Mali.
- Advances and challenges in malaria vaccine development.
- The Plasmodium falciparum-specific human memory B cell compartment expands gradually with repeated malaria infections.
- A prospective analysis of the Ab response to Plasmodium falciparum before and after a malaria season by protein microarray.
- In vitro growth-inhibitory activity and malaria risk in a cohort study in mali.
- Atypical memory B cells are greatly expanded in individuals living in a malaria-endemic area.
- Plasmodium falciparum signal peptide peptidase is a promising drug target against blood stage malaria.
- The TLR9 ligand CpG promotes the acquisition of Plasmodium falciparum-specific memory B cells in malaria-naive individuals.
- Sickle cell trait is associated with a delayed onset of malaria: implications for time-to-event analysis in clinical studies of malaria.
- The TLR9 agonist CpG fails to enhance the acquisition of Plasmodium falciparum-specific memory B cells in semi-immune adults in Mali.
- Assessment of mercury exposure and malaria in a Brazilian Amazon riverine community.
- A nested real-time PCR assay for the quantification of Plasmodium falciparum DNA extracted from dried blood spots.
Schools
Johns Hopkins University School of Medicine
Massachusetts General Hospital
National Institutes Of Health
Doctors Specialties
- Infectious Disease Medicine
- Infectious Disease
Accepted Insurances
Education
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National Institutes of Health Clinical Center -
Massachusetts General Hospital -
Johns Hopkins University School of Medicine
Helpful Reviews
Medicare Facts
| National Provider Identifier [NPI] | 1235120015 |
| Last Name Of The Provider | CROMPTON |
| First Name Of The Provider | PETER |
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