Phuong-Thu Pham1, Joanna Schaenman, Phuong-Chi Pham. 1. aDepartment of Medicine, Nephrology Division, David Geffen School of Medicine at UCLA, Kidney Transplant Program, Los Angeles bDepartment of Medicine, Division of Infectious Disease, David Geffen School of Medicine at UCLA, Los Angeles cDepartment of Medicine, Division of Nephrology and Hypertension, Olive View-UCLA Medical Center, Sylmar, California, USA.
Abstract
PURPOSE OF REVIEW: In recipients of kidney transplants, the emergence of BK virus (BKV)-associated clinical syndromes, such as viruria, viremia, and BK nephropathy, coincided with the advent of potent immunosuppressive therapy. There is currently no standardized protocol for the management of BK viruria or viremia, or established BK nephropathy. Suggested risk factors for BKV replication and a literature overview on various treatment strategies for BKV-associated clinical syndromes are presented, followed by the authors' proposed approach for screening, monitoring, and treatment of post-transplant BKV infection. RECENT FINDINGS: BKV infection can occur under all combinations of immunosuppressive therapy. Although both humoral and cellular immunity may be essential, BKV-specific T-cell immunity appears to play a pivotal role in controlling BKV replication. Monitoring BKV-specific immune response might prove useful in guiding therapeutic intervention. The beneficial effects of antiviral agents remain unclear. Development of T-cell or antibody-based vaccines against BKV is a subject of future research. SUMMARY: In the absence of conclusive evidence that any particular immunosuppressive agent has a specific influence over another on BKV infection risk and the unclear benefit of antiviral agents, intensive monitoring of serum BKV using PCR and immunological containment of BKV replication should remain the mainstay of therapy. The routine recommendations of antiviral agents in the treatment of BKV-associated clinical syndromes await results of large prospective randomized trials.
PURPOSE OF REVIEW: In recipients of kidney transplants, the emergence of BK virus (BKV)-associated clinical syndromes, such as viruria, viremia, and BK nephropathy, coincided with the advent of potent immunosuppressive therapy. There is currently no standardized protocol for the management of BK viruria or viremia, or established BK nephropathy. Suggested risk factors for BKV replication and a literature overview on various treatment strategies for BKV-associated clinical syndromes are presented, followed by the authors' proposed approach for screening, monitoring, and treatment of post-transplant BKV infection. RECENT FINDINGS:BKV infection can occur under all combinations of immunosuppressive therapy. Although both humoral and cellular immunity may be essential, BKV-specific T-cell immunity appears to play a pivotal role in controlling BKV replication. Monitoring BKV-specific immune response might prove useful in guiding therapeutic intervention. The beneficial effects of antiviral agents remain unclear. Development of T-cell or antibody-based vaccines against BKV is a subject of future research. SUMMARY: In the absence of conclusive evidence that any particular immunosuppressive agent has a specific influence over another on BKV infection risk and the unclear benefit of antiviral agents, intensive monitoring of serum BKV using PCR and immunological containment of BKV replication should remain the mainstay of therapy. The routine recommendations of antiviral agents in the treatment of BKV-associated clinical syndromes await results of large prospective randomized trials.
Authors: Susanna K Tan; Chunhong Huang; Malaya K Sahoo; Jenna Weber; Jason Kurzer; Margaret R Stedman; Waldo Concepcion; Amy E Gallo; Diane Alonso; Titte Srinivas; Gregory A Storch; Aruna K Subramanian; Jane C Tan; Benjamin A Pinsky Journal: J Infect Dis Date: 2019-07-02 Impact factor: 5.226
Authors: Michiel C van Aalderen; Ester B M Remmerswaal; Kirstin M Heutinck; Anja Ten Brinke; Mariet C W Feltkamp; Neelke C van der Weerd; Karlijn A M I van der Pant; Frederike J Bemelman; René A W van Lier; Ineke J M Ten Berge Journal: PLoS Pathog Date: 2016-10-10 Impact factor: 6.823