Current Environment: Production

Steven Siegel | Medical Services

Programs & Services

Languages

  • English

Steven Siegel | 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

Steven Siegel | Certifications

  • American Board of Pediatrics (General)

Steven Siegel | 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.

Steven Siegel | Publications

  1. Clearance of Pneumococcal Colonization in Infants Is Delayed through Altered Macrophage Trafficking. PLoS Pathog. 2015 Jun; 11(6):e1005004. View Clearance of Pneumococcal Colonization in Infants Is Delayed through Altered Macrophage Trafficking. Abstract

  2. Mechanisms of Bacterial Colonization of the Respiratory Tract. Annu Rev Microbiol. 2015; 69:425-44. View Mechanisms of Bacterial Colonization of the Respiratory Tract. Abstract

  3. TLR2 signaling decreases transmission of Streptococcus pneumoniae by limiting bacterial shedding in an infant mouse Influenza A co-infection model. PLoS Pathog. 2014 Aug; 10(8):e1004339. View TLR2 signaling decreases transmission of Streptococcus pneumoniae by limiting bacterial shedding in an infant mouse Influenza A co-infection model. Abstract

  4. Influenza promotes pneumococcal growth during coinfection by providing host sialylated substrates as a nutrient source. Cell Host Microbe. 2014 Jul 09; 16(1):55-67. View Influenza promotes pneumococcal growth during coinfection by providing host sialylated substrates as a nutrient source. Abstract

  5. TRIM protein-mediated regulation of inflammatory and innate immune signaling and its association with antiretroviral activity. J Virol. 2013 Jan; 87(1):257-72. View TRIM protein-mediated regulation of inflammatory and innate immune signaling and its association with antiretroviral activity. Abstract

  6. Activation of the mitogen-activated protein kinase, Slt2p, at bud tips blocks a late stage of endoplasmic reticulum inheritance in Saccharomyces cerevisiae. Mol Biol Cell. 2010 May 15; 21(10):1772-82. View Activation of the mitogen-activated protein kinase, Slt2p, at bud tips blocks a late stage of endoplasmic reticulum inheritance in Saccharomyces cerevisiae. Abstract

  7. RNase 1 genes from the family Sciuridae define a novel rodent ribonuclease cluster. Mamm Genome. 2009 Nov-Dec; 20(11-12):749-57. View RNase 1 genes from the family Sciuridae define a novel rodent ribonuclease cluster. Abstract

  8. Functionally competent eosinophils differentiated ex vivo in high purity from normal mouse bone marrow. J Immunol. 2008 Sep 15; 181(6):4004-9. View Functionally competent eosinophils differentiated ex vivo in high purity from normal mouse bone marrow. Abstract

  9. 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. J Immunol. 2007 Aug 01; 179(3):1693-9. View 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. Abstract

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