Steven Siegel, MD, PhD
Assistant in Pediatrics, Division of Infectious Diseases
Instructor of Pediatrics, Harvard Medical School
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Steven Siegel, MD, PhD
Assistant in Pediatrics, Division of Infectious Diseases
Instructor of Pediatrics, Harvard Medical School
Medical Services
Languages
English
Education
Graduate School
University of Pennsylvania
2014
Philadelphia
PA
Medical School
University of Pennsylvania
2016
Philadelphia
PA
Residency
Pediatrics, Accelerated Research Pathway
Boston Children's Hospital
2018
Boston
MA
Fellowship
Pediatric Infectious Diseases
Boston Children's Hospital
2022
Boston
MA
Certifications
American Board of Pediatrics (General)
Professional History
After completing combined MD and PhD training at the University of Pennsylvania, Dr. Siegel moved to Boston for pediatric residency at Boston Children's Hospital and Boston Medical Center in the accelerated research pathway. He then remained at Boston Children's Hospital for pediatric infectious diseases fellowship training, and joined the division faculty in 2022. He has a clinical interest in immunocompromised patients, particularly those who have undergone hematopoietic stem cell transplant (HCT). He conducts research in the laboratories of Drs. Seth Rakoff-Nahoum and Leslie Kean on the impact of the gut microbiome on outcomes in HCT patients.
Publications
Clearance of Pneumococcal Colonization in Infants Is Delayed through Altered Macrophage Trafficking. View Abstract
Mechanisms of Bacterial Colonization of the Respiratory Tract. View Abstract
TLR2 signaling decreases transmission of Streptococcus pneumoniae by limiting bacterial shedding in an infant mouse Influenza A co-infection model. View Abstract
Influenza promotes pneumococcal growth during coinfection by providing host sialylated substrates as a nutrient source. View Abstract
TRIM protein-mediated regulation of inflammatory and innate immune signaling and its association with antiretroviral activity. View Abstract
Activation of the mitogen-activated protein kinase, Slt2p, at bud tips blocks a late stage of endoplasmic reticulum inheritance in Saccharomyces cerevisiae. View Abstract
RNase 1 genes from the family Sciuridae define a novel rodent ribonuclease cluster. View Abstract
Functionally competent eosinophils differentiated ex vivo in high purity from normal mouse bone marrow. View Abstract
Eosinophils from lineage-ablated Delta dblGATA bone marrow progenitors: the dblGATA enhancer in the promoter of GATA-1 is not essential for differentiation ex vivo. View Abstract