PIPages
Labs

Scott Pegan

University of California-Riverside, CA·Microbiology & Immunology

Some tick-borne viruses in the nairovirus group cause serious illness in people and livestock, and no licensed vaccine or preventive drug exists for any of them. The best known, Crimean-Congo hemorrhagic fever virus, is present across parts of Europe, Asia and Africa, and both the virus and its tick carriers have been appearing in areas where they were previously absent.

Fields

Microbiology & Immunology

Biochemistry

Medicine & Clinical Research

Topics

Crimean-Congo hemorrhagic fever

nairovirus

bunyavirus

Grants
1 known grant, through Aug 2030

What they work on

  1. Define how non-neutralizing monoclonal antibodies against GP38, a non-structural glycoprotein of Crimean-Congo hemorrhagic fever virus, confer protection, using combined molecular, cell-based and animal approaches.
  2. Determine the protective contribution of antibody responses to the nairovirus nucleoprotein, the protein that packages the viral genome, as suggested by earlier replicon-particle protection studies.
  3. Isolate monoclonal antibody candidates from people who survived infection, screening for high efficacy and for cross-protection against related nairoviruses such as Nairobi sheep disease, Erve, Songling and Yezo viruses.
  4. Translate mechanistic findings on these two viral proteins into antigen and antibody strategies suitable for further preclinical and clinical testing.

More about the research

Related nairoviruses, including the agents of Nairobi sheep disease and the more recently described Songling and Yezo viruses, cause human or animal disease of varying severity with economic costs. Understanding which parts of the immune response actually protect is the bottleneck for developing countermeasures.

Why it matters

There is currently no vaccine or preventive treatment for Crimean-Congo hemorrhagic fever or other nairovirus diseases, which can be fatal in a large share of cases and also affect livestock. Clarifying how protective antibodies work, and identifying candidates from survivors, could support development of broadly protective antibody therapies and vaccine designs for patients and for regions where these viruses are spreading.

Known grants

From NIH and NSF research grants. Labs often have other funding we can't see.

Identification of GP38 and NP antibodies and their protective mechanisms against CCHFV

NIH · Sep 2025 – Aug 2030

Closest labs

Anthony Bowen

Columbia University, NY·Microbiology & Immunology·Early-career

Test whether immune imprinting from an initial D614G-strain vaccination limits neutralizing antibody responses to Omicron BA.4/5 boosters, using controlled immunization schedules in humanized mice that generate human-like antibodies.

Justin Bailey

Johns Hopkins University, MD·Microbiology & Immunology

Test whether a dengue vaccine's serotype composition determines the balance, neutralizing potency, and durability of serotype-specific versus cross-reactive memory B cells and monoclonal antibodies, and whether those responses predict protection after controlled human challenge with serotype 2.

Meghan Hermance

University of South Alabama, AL·Microbiology & Immunology

Characterize how severe fever with thrombocytopenia syndrome virus (SFTSV) infects, spreads within and survives molting in Haemaphysalis longicornis ticks, including which tick cell types it infects across life stages.

The school

University of California-Riverside: 21 labs on PI Pages, $232M a year on research, 328 research doctorates a year.

More about University of California-Riverside

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