Transplacental Transmission of RSV (TTRSV)

A Prospective Cohort Study Evaluating the Transplacental Transmission of Respiratory Syncytial Virus (RSV) in Pregnant Women and Their Offspring

Aim 1: To study transplacental transmission of Respiratory Syncytial Virus (RSV) and how this is moderated by other maternal infections during pregnancy

Aim 2: To test maternal blood for presence of RSV-specific immunoglobulins and how this is moderated by other maternal infections during pregnancy

Aim 3: To test cord blood (fetal blood) for presence of RSV-specific immunoglobulins and other common viral pathogens

Aim 4: To perform further tests (Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR), Droplet Digital Polymerase Chain Reaction (ddPCR) and immunoprobing) to confirm the presence of RSV and other common viral pathogens

Aim 5: To follow these newborn infants up to 4 years of age to look for redisposition to respiratory diseases and growth parameters

Study Overview

• Status: Active, not recruiting
• Conditions: Asthma; Bronchiolitis; Respiratory Syncytial Virus (RSV); SARS CoV 2 Infection

Detailed Description

Patients will be consented at one of two time points during their pregnancy. Option 1: If mothers present or call Obstetrics and Gynecology (OB) with signs or symptoms of an Upper Respiratory Infection (URI) and or a positive SARS-CoV-2 test, the mother's OB will ask if the mother would be interested in hearing about this study at her next prenatal visit if study personnel are not available to discuss the study at the present appointment. If study personnel is available and on-site, they will approach and consent patients who meet criteria after preliminary screening.

Option 2: Mothers who present to labor and delivery and report a history of an URI in the last three weeks and or a history of positive SARS-CoV-2 will be asked by the labor and delivery team or study personnel, if available, about her interest in the study and approached for consent upon admission to labor and delivery. At the time of consent a research blood sample will be drawn if the patient is not already having labs drawn, if the mother agrees.

The additional data collection will be performed electronically. Research staff will contact participants (in person, via email, and via phone, depending on survey timing). REDCap will be used for data collection, with (offline, when necessary) electronic data capture. Participants can access an online version of surveys using their own device or phone, or use tablets provided for the participants for data collection at the hospitals. Participant will have the option to have research staff conduct the question/interview in-person or over the telephone, if this is preferred.

If the mother is enrolled prior to labor, study personnel will then track the enrolled subject's admission to the labor and delivery unit using the electronic health records and regular contact with the OB/GYN service. Study personnel will determine if the subject still meets enrollment criteria after admission to labor and delivery (e.g., baby was carried to at least near full term (34 weeks and beyond) and delivered at either Lakeside Hospital and Clinic or Ochsner Baptist Medical Center). If the patient is still eligible for the study, the study personnel will liaise with bedside nursing to have the maternal research samples collected at the same time standard of care samples are being drawn.

Cord (i.e., fetal) blood, placental tissue, and the newborn naso-pharyngeal aspirate fluid will be collected as early as possible after delivery. All samples will undergo microbiological analyses using Enzyme-Linked Immunoassay (ELISA), Polymerase Chain Reaction (PCR) and CRISPR testing to identify evidence of previous or current infection.

Patients will be given the option of allowing the study team to deidentify and store any remaining maternal and/or infant specimens for additional testing.

Patients will be given the option to allow the study team member to store de-identified remaining maternal and/or infant specimens for future studies.

Patients will be given the option to allow the research team to contact them about their enrollment in any future studies.

All study visits after the collection of biological samples at delivery will be done remotely, through a review of the infant's electronic medical records and questionnaires completed over the phone or via other electronic media (e.g. Zoom) as determined by maternal preference. Mothers will provide information via the use of structured questionnaires delivered and returned by mail every 6 months or by phone based on maternal preference. Telephone interviews and mailed questionnaires will have questions regarding respiratory-related symptoms and diagnoses, allergies, and medications for the index child.

• Study Type: Observational
• Enrollment (Actual): 300

Contacts and Locations

Study Locations

• United States
  • Louisiana
    • Metairie, Louisiana, United States, 70001
      • Tulane University Lakeside Hospital
    • New Orleans, Louisiana, United States, 70115
      • Ochsner Baptist Hospital

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 14 years and older (Adult, Older Adult)
• Accepts Healthy Volunteers: Yes

• Sampling Method: Probability Sample

Study Population

Pregnant women who plan to deliver at Tulane Lakeside Hospital and Clinic and Ochsner Baptist Medical Center will be considered for inclusion in the study. Pregnant women and their infants who fulfill all inclusion criteria are eligible for participation.

Description

Inclusion Criteria:

1. Aged 18 years or older;
2. Reported 2 or more signs and symptoms of respiratory infection during pregnancy, including but not limited to: fever, nasal congestion/discharge, cough, and sore throat and/or a positive SARS-CoV-2 test
3. Deliveries at full term or near term (minimum 34 weeks gestation) in Labor and Delivery (L&D) facilities at Tulane Lakeside Hospital and Clinic or Ochsner Baptist Medical Center who were pregnant during RSV season.
4. History negative for Human Immunodeficiency Virus (HIV)
5. No use of immunosuppressive medications/therapies.
6. Singleton gestation;
7. Willing to allow for follow up of the child via their medical record from the time of delivery to 4 years of age.
8. Clearly understands the study procedures and visit schedule, alternative treatments, and risks involved with the study, and voluntarily agrees to participate by giving written informed consent.
9. English or Spanish proficiency

Exclusion Criteria:

1. Under 18 years of age at the time of consent.
2. Gestational age less than 12.0 weeks at the time of consent.
3. Does not report at least 2 of the following signs and symptoms of respiratory infection during pregnancy, including but not limited to: fever, nasal congestion/discharge, cough, and sore throat.
4. Positive medical history for HIV.
5. Current use of immunosuppressive therapies/drugs.
6. Newborn has been diagnosed with congenital abnormality or chronic disease at birth.
7. Unwilling or unable to provide written informed consent.
8. Mother was not pregnant during the RSV season or no positive SARS-CoV-2 test during pregnancy.
9. Subject is unwilling to allow for follow up of the child via medical records from the time of delivery to 4 years of age;
10. Multiple birth;
11. Lacks English or Spanish proficiency

Infants will be excluded from the study in the event of a Serious Adverse Event such as fetal or acute neonatal death (in the delivery room) if the mother does not provide clinical consent for an autopsy.

Study Plan

How is the study designed?

Design Details

• Observational Models: Cohort
• Time Perspectives: Prospective

Number of groups / cohorts

4

Cohorts and Interventions

Group / Cohort
Mother infected/newborn not infected
Mother infected/newborn infected
Mother not infected/newborn not infected
Mother not infected/newborn infected

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Postnatal respiratory morbidity	The investigators will monitor the offspring via electronic medical records and mailed questioners to record respiratory symptoms such as upper respiratory infections, cough, wheezing.	5 Years
Passage of antiviral antibodies from mother to newborn	The investigators will assess the antiviral protection provided by maternal fetal transport of neutralizing antibodies following maternal vaccination versus natural infection.	5 Years
Vertical transmission of RSV and/or SARS-COV2 from infected mother to the offspring	The investigators will use PCR to detect the presence of each virus in maternal blood and cord blood.	5 Years

Collaborators and Investigators

• Sponsor: Tulane University
• Collaborators: National Institutes of Health (NIH)
• Investigators: Principal Investigator: Giovanni Piedimonte, MD, FAAP, FCCP, Tulane University

Study record dates

Study Major Dates

• Study Start (Actual): May 25, 2020
• Primary Completion (Estimated): August 1, 2027
• Study Completion (Estimated): August 1, 2028

Study Registration Dates

• First Submitted: June 29, 2022
• First Submitted That Met QC Criteria: June 29, 2022
• First Posted (Actual): July 5, 2022

Study Record Updates

• Last Update Posted (Actual): May 20, 2026
• Last Update Submitted That Met QC Criteria: May 18, 2026
• Last Verified: May 1, 2026

More Information

Terms related to this study

• Keywords: COVID-19; Fetal blood
• Additional Relevant MeSH Terms: Immune System Diseases; Respiratory Tract Infections; Infections; RNA Virus Infections; Virus Diseases; Respiratory Tract Diseases; Lung Diseases; Bronchial Diseases; Lung Diseases, Obstructive; Respiratory Hypersensitivity; Hypersensitivity, Immediate; Hypersensitivity; Pneumonia, Viral; Pneumonia; Coronavirus Infections; Coronaviridae Infections; Nidovirales Infections; Bronchitis; COVID-19; Asthma; Bronchiolitis
• Other Study ID Numbers: 2019-1517

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No