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This Combined Synopsis/Solicitation opportunity from Department Of Health And Human Services was posted on August 11, 2026. The submission period has ended. Browse the details below for market research, or find similar active opportunities.

Notice of Intent to Sole Source: West Virginia University Research Corporation

Awarded
98769Federal

Contract Overview

Solicitation details, issuing organization, response deadlines, documents, and interested companies for this government contract opportunity.

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AI Contract Overview

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The CDC Office of Acquisition Services is issuing a Notice of Intent to Sole Source for the West Virginia University Research Corporation under solicitation 98769. This project focuses on evaluating the health risks associated with respirable crystalline silica found in engineered stone countertops, specifically investigating the link between dust exposure during fabrication and the development of autoimmune diseases. The research aims to clarify the underlying mechanisms of these responses through animal studies involving oropharyngeal aspiration in mice. The study will utilize 48 mice across two strains, NZBWF1/J and C57BL/6J, to test the effects of two different engineered stone variants, Silestone and HybriQ, against a control group. Performance of the research will take place in Morgantown, West Virginia. The solicitation was posted on August 11, 2026, with a response deadline of August 21, 2026.

General Info

CDC sole source contract for WVU to study engineered stone silica health risks.

NAICS

541714 - Research and Development in Biotechnology (except Nanobiotechnology)

Place of Performance

Morgantown, WV, 26506, USA

Set-Aside

NONE

Documents

1

Sole Source Justification for Research Services at WVU

PDF, High priority: read this firstjustification-and-authorization
High

AI Contract Breakdown

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Timeline

PhaseAwarded
Posted

Combined Synopsis

Awarded

Contract was awarded

Submission Closed

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Organization & Contact Information

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AgencyDepartment Of Health And Human Services → CDC Office Of Acquisition Services
Contacts1 person available
OfficeATLANTA, GA, 30333, USA
Office AddressATLANTA, GA, 30333, USA
Contacts

Full Description

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Engineered stone countertops containing more than 90% crystalline silica have become increasingly popular among consumers in recent years. As a result, the rapidly growing workforce in this industry is at significant risk of a well-documented occupational hazard—overexposure to respirable crystalline silica (RCS), which can lead to progressive, irreversible, and potentially disabling pulmonary silicosis. Epidemiological studies have also linked occupational exposure to RCS with the occurrence of autoimmune diseases, including lupus erythematosus, systemic sclerosis, and rheumatoid arthritis. However, the relationship between the development of these autoimmune diseases and silica-induced inflammation and fibrosis remains unclear, and the underlying mechanisms of RCS-induced autoimmune responses have not been fully elucidated. This study hypothesizes that dust from engineered stone fabrication may cause serious health issues, especially triggering autoimmune responses. To test this hypothesis, animal studies are required. This project involves oropharyngeal aspiration studies to evaluate autoimmune responses to chronic exposure to emissions from engineered stone materials in mice. The project was initiated at CDC/NIOSH/HELD in 2024 and paused in 2025. The overall objective of this project is to evaluate the immune responses to dust released from engineered stone countertops during fabrication processes in mice to better understand worker health risks associated with these exposures. This study will employ a sensitization and challenge model to evaluate autoimmune responses following repeated exposure to engineered stone dust. To determine engineered stone dust (ESD)–induced autoimmune responses in mice, two strains of mice (NZBWF1/J and C57BL/6J) will be exposed to two ESD variants—Silestone (~90% crystalline silica) and HybriQ (~60% crystalline silica)—with evaluation at 90 days post-exposure. The study design will include two mouse strains, two ESD variants, and three exposure groups (Silestone, HybriQ, and PBS control), with 8 mice per group and a single exposure dose, followed by a 90-day post-exposure period. The total number of mice is 48 (24 NZBWF1/J and 24 C57BL/6J).

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