NIAID-Supported Research is Advancing the Response to Surging Syphilis Rates

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Syphilis, a common sexually transmitted infection (STI) caused by the bacteria Treponema pallidum, is a centuries-old STI that can result in adult neurological and organ damage, as well as congenital abnormalities, stillbirths, and neonatal deaths. Benzathine penicillin G (BPG) was introduced as syphilis treatment in the middle of the 20th century and led to a precipitous drop in disease burden, but T. pallidum continues to circulate in the global population, including in the United States. U.S. syphilis incidence has increased since 2000, marked by a sharp rise in reported adult and congenital cases since 2019 and, notably, an escalating toll in medically underserved populations. There is currently a shortage of BPG, which is still one of only a few antibiotics known to effectively treat syphilis. There is no preventive vaccine and most syphilis testing is done in a laboratory setting, which prevents people from learning their status conveniently and in real time. More research is urgently needed to diversify the diagnostic, preventive, and therapeutic options available to alter the course of the growing public health threat of syphilis. NIAID supports a research portfolio to help address these areas of need, including studies featured at the recent STI & HIV World Congress in Chicago.  

Updates from STI & HIV World Congress

The STI & HIV World Congress hosted presentations on new STI research, policy, and public health implementation issues, and was attended by a global community of scientists, policymakers, healthcare providers, advocates and community organizations. NIAID-supported studies and research priorities presented at the meeting included an update on syphilis vaccine development, an overview of strategies for enhanced penicillin allergy screening, exploratory research to identify new syphilis therapeutics, and the latest data and next steps to explore the utility of the antibiotic doxycycline as post-exposure prophylaxis for syphilis and other STIs—an approach commonly referred to as DoxyPEP:

  • Lorenzo Giacani, Ph.D., from the University of Washington as well as Alloysius Gomez, B.Sc. and Simon Houston, Ph.D., from the University of Victoria described results from NIAID-supported syphilis vaccine studies, including preclinical (animal) research showing a vaccine containing three different antigens—a protein and peptides from the surface of T. pallidum bacteria—enabled animals to mount an immune response when they subsequently acquired syphilis, experiencing reduced severity of disease, but not full protection from infection. Dr. Houston shared how a laboratory team identified 95% of the approximately 1,000 proteins in T. pallidum. This discovery may enable scientists to select one or more of those proteins as targets for future vaccine candidates.
  • Approximately 15% of people attending STI clinics report an allergy to penicillin, which prevents them from using the preferred BPG treatment. However, previous studies have shown more than 95% of people who self-reported penicillin allergy could safely use the antibiotic, according to allergy test results. Rebecca Lillis, M.D., from the Louisiana State University School of Medicine, shared a validated process for determining penicillin allergy status in an STI care setting, which would enable providers to safely clear people who previously reported penicillin allergy for use of BPG.
  • Given the limited known treatments for syphilis, Virginia Tech Ph.D. candidate Kathryn Hayes presented results of a study to screen more than 100 β-lactams—antibiotics in the same class as penicillin—for their ability to kill T. pallidum bacteria or slow their growth. The team identified multiple β-lactams showing higher efficacy than BPG against T. pallidum in the laboratory, which may inform future research to develop new syphilis therapeutics.
  • Multiple presenters addressed emerging NIAID-supported science on the use of DoxyPEP for STIs, including Connie Celum, M.D., M.P.H., from the University of Washington-Fred Hutch, Annie Luetkemeyer, M.D., from the University of California San Francisco, and Jenell Stewart, D.O., M.P.H., from the University of Minnesota. Presenters reviewed the high efficacy of DoxyPEP in preventing syphilis, gonorrhea, and chlamydia among men who have sex with men and transgender women, as well as the need to understand whether the lower efficacy observed in cisgender women to date may be due to lower acceptability of DoxyPEP in that population, which could pose a barrier to taking doxycycline as prescribed. Presenters underscored the need for further research and vigilance with respect to antimicrobial resistance and STI testing, the latter due to the potential for a false negative test result while someone is taking DoxyPEP.

Current and Future NIAID Syphilis Research

In addition to the latest findings presented at the conference, new and ongoing NIAID-supported studies are helping to close gaps in the current syphilis response. To address the complicated and limited diagnostic tools currently available for syphilis, a new NIAID-supported study is enrolling volunteers at all stages of infection to provide laboratory samples for a biorepository of syphilis specimens. This biorepository will safely avail high-quality syphilis specimens for laboratories to use as they create new diagnostics. A new complementary funding opportunity will advance development of promising diagnostic technologies for congenital and adult syphilis.

The new Syphilis in Pregnancy Study (SIPS) is monitoring the outcomes of pregnant people diagnosed with and treated for syphilis, as well as the health outcomes of their infants. SIPS is expected to shed light on how adult and infant immune systems respond with effective treatment. Results may inform development of future vaccine concepts that could stimulate a similar immune response when a person is initially exposed to syphilis, thereby preventing infection.

In addition, NIAID funds STI cooperative research centers (CRCs) to advance the science related to numerous STIs, including development of syphilis vaccine concepts. In their pursuit of a syphilis vaccine, the CRCs are investigating the structure of proteins on the outer membrane (layer) of T. pallidum bacteria as potential vaccine targets and developing the tri-antigen vaccine that was featured at the STI & HIV World Congress. NIAID plans to fund new CRC awards in 2024.

Finally, in recognition of the limited treatment options for syphilis, the low-but-significant prevalence of penicillin allergy, and the current drug shortage, NIAID is soliciting small business contract proposals for identification of alternatives to BPG for syphilis treatment.

Syphilis is a serious public health challenge. Scientific discovery, research and development will continue to play a critical role in enabling an equitable and effective response to the syphilis surge.

References:

C Celum. STI biomedical prevention in 2023: Doxy PEP and Beyond. Presentation at the STI & HIV 2023 World Congress in Chicago, Illinois. Wednesday, July 26, 2023.

L Giacani. State of syphilis vaccine development. Presentation at the STI & HIV 2023 World Congress in Chicago, Illinois. Tuesday, July 25, 2023.

A Gomez. Syphilis vaccine development: Generating a stable and efficacious multi-epitope vaccine chimera through protein engineering. Presentation at the STI & HIV 2023 World Congress in Chicago, Illinois. Wednesday, July 26, 2023.

KA Hayes. A large-scale drug screen identifies novel therapeutics that target the syphilis pathogen Treponema pallidum. Presentation at the STI & HIV 2023 World Congress in Chicago, Illinois. Wednesday, July 26, 2023.

S Houston. Treponema pallidum Proteomic Analysis to Inform Syphilis Vaccine Development. Presentation at the STI & HIV 2023 World Congress in Chicago, Illinois. Wednesday, July 26, 2023.

A Luetkemeyer. Doxycycline Post-exposure prophylaxis (PEP) & PrEP for Syphilis Prevention. Presentation at the STI & HIV 2023 World Congress in Chicago, Illinois. Thursday, July 27, 2023.

RA Lillis. Validation of an Easy to Administer Algorithm to Define Penicillin Allergy Status in STI Clinic Outpatients. Presentation at the STI & HIV 2023 World Congress in Chicago, Illinois. Wednesday, July 26, 2023.

J Stewart. Self-reported adherence to event-driven doxycycline postexposure prophylaxis for sexually transmitted infection prevention among cisgender women. Presentation at the STI & HIV 2023 World Congress in Chicago, Illinois. Tuesday, July 25, 2023.

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Provide Input on NIH Herpes Simplex Virus Strategic Plan

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NIAID, along with multiple other NIH institutes and centers, invites comments and input from stakeholders throughout the scientific research community and the general public on a Herpes Simplex Virus (HSV) Strategic Plan structured around four key strategic approaches detailed below:

Strategic Priorities

Priority 1: Improve fundamental knowledge of HSV biology, pathogenesis, and epidemiology

  • Enhance fundamental knowledge of HSV biology, including viral interactions with host cells and mechanism of replication and transport; fundamental aspects of innate and adaptive immune response to HSV; HSV disease pathogenesis in multiple organ systems, including the skin, reproductive tract, eye, and the peripheral and central nervous systems; and the key drivers of disease transmission.
  • Characterize host and pathogen drivers that underlie dynamics of HSV latency and reactivation.
  • Improve understanding of diverse pathophysiology of HSV infection including neonatal infection and the role of mucosal immunity to reduce genital and orolabial infection and disease; and a deeper understanding of the neurologic impact of HSV infection, including herpes simplex encephalitis, and post-associations with neurodegenerative disorders such as Alzheimer’s disease.
  • Explore epidemiology of and co-morbidities associated with HSV infection.
  • Improve and develop new in vitro and in vivo models that reflect human disease.

Priority 2: Accelerate research to improve diagnosis

  • Develop improved biomarkers and technologies for herpes diagnosis.
  • Improve sensitivity and specificity of serologic tests that can be made commercially.
  • Support research to improve point-of-care diagnostics.

Priority 3: Improve strategies to treat and cure HSV

  • Support research to identify immune correlates of protection for HSV1 and HSV2.
  • Advance the development of promising prophylactic vaccines.
  • Support clinical trials to test new evaluation of therapies, diagnostics, and vaccines (therapeutic and prophylactic).

Priority 4: Advanced research to prevent HSV infection

  • Support research to identify immune correlates of protection for HSV1 and HSV2.
  • Advance the development of promising prophylactic vaccines.
  • Support clinical trials to test new evaluation of therapies, diagnostics, and vaccines (therapeutic and prophylactic).

Information Requested

What is your view of NIH’s strategic plan for HSV research? NIH wants your feedback on the following regarding the proposed framework above.

  • What significant research gaps or barriers are not identified in the strategic priorities?
  • What are the necessary resources critical to advancing research in the strategic priorities?
  • Are there any emerging scientific advances or techniques that may accelerate research related to the strategic priorities?
  • Could other approaches advance treatment and prevention of HSV? What are possible future priority areas for new clinical research?

How to Submit Responses

Submit all comments electronically on the RFI website by 11:59 p.m. Eastern Time on June 21, 2023. Do not include any personally identifiable information that you do not wish to make public, including proprietary, classified, confidential, trade secret, or sensitive information.

Direct all inquiries to NIHHSVResearch@niaid.nih.gov.

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NIH-Funded Study Finds Doxycycline Reduces Sexually Transmitted Infections by Two-Thirds

The oral antibiotic doxycycline prevented the acquisition of sexually transmitted infections (STIs) when tested among study participants who took the medication within 72 hours of having condomless sex. The post-exposure approach, termed doxy-PEP, resulted in a two-thirds reduction in the incidence of syphilis, gonorrhea, and chlamydia among the study participants.

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Develop Vaccine Candidates for Sexually Transmitted Infections (STIs)

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NIAID seeks applicants who can develop advanced vaccines for STI pathogens that have limited candidates in the product development pipeline through the new request for applications (RFA) Sexually Transmitted Infections (STI) Cooperative Research Centers (CRC) Vaccine Development (U01, Clinical Trial Not Allowed).

Research Objectives

The goal of this RFA is to identify and support feasible vaccine candidates, regardless of source. While NIAID’s Division of Microbiology and Infectious Diseases has made substantial investment in STI vaccine development, this initiative will focus on advanced vaccine development for STI pathogens that have limited candidates in the product development pipeline: Neisseria gonorrhoeae, Chlamydia trachomatis, and Treponema pallidum.

For your application, you will need to provide a Product Development Strategy (PDS) in addition to a Research Plan. The PDS should discuss Milestones and Timelines for product development; the intended use/indication of the proposed product; and the value of the product compared to existing products. The PDS may look beyond those planned activities described in the Research Plan, which is constrained by the RFA’s budget and project period limitations.

Though not required, we strongly encourage you to partner with relevant industry expertise as you develop your application and, if successful, collaborate on the performance of the research project (e.g., establish a subaward). An industry partner can provide knowledge of product development planning, product profile development, and regulatory matters. Consider retaining such support through defined personnel effort or plan for periodic consultation on specific issues.

Below are examples of advanced vaccine development activities that align with NIAID’s research areas of interest:

  • Toxicology
  • Clinical assay development
  • Formulation
  • Process development and control assays
  • Good manufacturing practice

Additionally, avoid proposing the following research areas in your application or NIAID will consider the application nonresponsive and not review it:

  • Vaccine development for pathogens other than: Neisseria gonorrhoeae, Chlamydia trachomatis, and Treponema pallidum
  • HIV/AIDS-related research
  • Clinical trials—refer to NIH’s Definition of a Clinical Trial

Budget Information and Deadline

Application budgets should not exceed $1.4 million in annual direct costs and should reflect the actual needs of the project. The scope of the proposed project should determine the project period which cannot exceed 5 years.

Applications are due on June 14, 2023, by 5 p.m. local time of the applicant organization.

Contact Information

Direct any inquiries to NIAID’s scientific/research contact, Dr. Thomas Hiltke, at thiltke@mail.nih.gov or 240-627-3275. Direct any peer review inquiries to Dr. Scott Jakes at scott.jakes@nih.gov or 240-220-1737.

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Viral Shedding Ebbs Over Time with HSV-1 Genital Infections

Biomedical Sciences Researcher Gets $4.9 Million Federal Grant to Study Ways to Block Gonorrhea Infection

Media Type
Article
Publish or Event Date
Research Institution
Georgia State University
Short Title
Biomedical Sciences Researcher Gets $4.9 Million Federal Grant to Study Ways to Block Gonorrhea Infection
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Content Manager

David (Ted) Hackstadt, Ph.D.

Education:

Ph.D., Washington State University

David (Ted) Hackstadt, Ph.D.

Mattia Bonsignori, M.D., M.S.

Education:

M.D., M.S., University of Insubria Medical School, Varese, Italy

Mattia Bonsignori, M.D., M.S.

Jeffrey I. Cohen, M.D.

Provides direct clinical care to patients at NIH Clinical Center

Education:

M.D., Johns Hopkins University

Jeffrey I. Cohen, M.D.

Helen C. Su, M.D., Ph.D.

Specialty(s): Allergy and Immunology, Pediatrics
Provides direct clinical care to patients at NIH Clinical Center

Education:

M.D., Ph.D., Brown University

photo of Helen Su, M.D., Ph.D.