Volume 56, Issue 1 pp. 215-222
TRANSFUSION COMPLICATIONS

Probable and possible transfusion-transmitted dengue associated with NS1 antigen–negative but RNA confirmed-positive red blood cells

Desiree Matos

Desiree Matos

American Red Cross Blood Services Region and

Search for more papers by this author
Kay M. Tomashek

Kay M. Tomashek

Dengue Branch, Centers for Disease Control and Prevention, San Juan, Puerto Rico

Search for more papers by this author
Janice Perez-Padilla

Janice Perez-Padilla

Dengue Branch, Centers for Disease Control and Prevention, San Juan, Puerto Rico

Search for more papers by this author
Jorge Muñoz-Jordán

Jorge Muñoz-Jordán

Dengue Branch, Centers for Disease Control and Prevention, San Juan, Puerto Rico

Search for more papers by this author
Elizabeth Hunsperger

Elizabeth Hunsperger

Dengue Branch, Centers for Disease Control and Prevention, San Juan, Puerto Rico

Search for more papers by this author
Kalanthe Horiuchi

Kalanthe Horiuchi

Division of Vector-Borne Disease Information Technology Support, Centers for Disease Control and Prevention, Fort Collins, Colorado

Search for more papers by this author
David Noyd

David Noyd

Dengue Branch, Centers for Disease Control and Prevention, San Juan, Puerto Rico

Search for more papers by this author
Colleen Winton

Colleen Winton

American Red Cross Scientific Support Office, Gaithersburg, Maryland

Search for more papers by this author
Gregory Foster

Gregory Foster

American Red Cross Scientific Support Office, Gaithersburg, Maryland

Search for more papers by this author
Marion Lanteri

Marion Lanteri

Blood Systems Research Institute, San Francisco, California

Search for more papers by this author
Jeffrey M. Linnen

Jeffrey M. Linnen

Hologic, San Diego, California

Search for more papers by this author
Susan L. Stramer

Corresponding Author

Susan L. Stramer

American Red Cross Scientific Support Office, Gaithersburg, Maryland

Address reprint requests to: Susan L. Stramer, PhD, American Red Cross, 9315 Gaither Road, Gaithersburg, MD 20877; e-mail: [email protected].Search for more papers by this author
First published: 07 September 2015
Citations: 38

Abstract

BACKGROUND

In the absence of active blood donation screening, dengue viruses (DENV) have been implicated in only a limited number of transfusion transmissions worldwide. This study attempted to identify if blood from donors testing negative by an NS1-antigen (Ag) enzyme-linked immunosorbent assay (ELISA) but confirmed positive for DENV RNA caused DENV-related disease in recipients during the epidemic years of 2010 to 2012 in Puerto Rico.

STUDY DESIGN AND METHODS

Donation aliquots testing negative by an investigational NS1-Ag ELISA were stored frozen and retested retrospectively using a research transcription-mediated amplification assay (TMA) detecting DENV RNA. All RNA-reactive donations were subject to confirmatory RNA and antibody testing. Recipient tracing was conducted for all components manufactured from TMA-reactive components. Medical chart review, recipient interview, and follow-up sampling occurred for 42 recipients transfused with TMA-reactive components.

RESULTS

Six of 42 recipients developed new-onset fever in the 2 weeks posttransfusion; three (50%) received RNA confirmed-positive, NS1-Ag–negative red blood cell (RBC) units. One recipient of a high-titer unit (7 × 107 DENV-4 RNA copies/mL) developed severe dengue, and a second recipient had only fever recorded but had a negative sepsis work-up. New fever attributable to DENV infection in a third recipient was confounded by fever potentially attributable to posttransfusion sepsis.

CONCLUSIONS

In our retrospective study, NS1-Ag detected 20% of all RNA confirmed-positive donations demonstrating limitations of NS1-Ag ELISA for blood donation screening. We identified one recipient with a clinical syndrome compatible with severe dengue who had received an NS1-Ag–negative but RNA confirmed-positive RBC unit. This investigation illustrates the difficulty in confirming transfusion transmission in dengue-endemic areas among severely ill transfusion recipients.

The full text of this article hosted at iucr.org is unavailable due to technical difficulties.