Journal of Global Infectious DiseasesOfficial Publishing of INDUSEM and OPUS 12 Foundation, Inc. Users online:529  
Print this pageEmail this pageSmall font sizeDefault font sizeIncrease font size     
Home About us Editors Ahead of Print Current Issue Archives Search Instructions Subscribe Advertise Login 
 


 
   Table of Contents     
LETTER TO EDITOR  
Year : 2016  |  Volume : 8  |  Issue : 4  |  Page : 161-162
Hepatitis A vaccine response in human immunodeficiency virus-infected patients: The interchangeability of single dose versus double: A prospective look


Department of Infectious Diseases, New York Medical College, Saint Michael's Medical Center, Newark, NJ 07102, USA

Click here for correspondence address and email

Date of Web Publication10-Nov-2016
 

How to cite this article:
Dazley J, Sison R, Jimenez H, Slim J. Hepatitis A vaccine response in human immunodeficiency virus-infected patients: The interchangeability of single dose versus double: A prospective look. J Global Infect Dis 2016;8:161-2

How to cite this URL:
Dazley J, Sison R, Jimenez H, Slim J. Hepatitis A vaccine response in human immunodeficiency virus-infected patients: The interchangeability of single dose versus double: A prospective look. J Global Infect Dis [serial online] 2016 [cited 2019 Sep 17];8:161-2. Available from: http://www.jgid.org/text.asp?2016/8/4/161/192965


Sir,

Hepatitis A virus (HAV) infection is problematic in HIV-infected patients. Comparison of single-antigen hepatitis A (HAVRIX) or double-antigen combined hepatitis A and hepatitis B (TWINRIX) vaccines showed better results in HIV-positive patients who received TWINRIX than those who received HAVRIX, depending on CD4 count. There is literature that indicates that the seroconversion rate is dependent on dose,[1],[2] which is our focus. We report the rate of seroconversion in HIV patients of various levels of immunocompromised state in those given different doses of vaccine. This was a prospective, randomized, nonblinded, single-center study at an urban ambulatory care HIV clinic directed at giving primary and HIV-specific care. Patients were included in the study if they had either a single or double dose of hepatitis vaccine. Antibodies for HAV were measured pre- and post-vaccination using the Vitros ECi immunodiagnostic system through the Laboratory Corporation of America (LabCorp). A positive test includes an antibody cutoff of <0.80 for anti-HAV total antibodies and a no detection of anti-HAV IgM at a cutoff of <0.80. Fisher's exact test was used for categorical variables in relation to antibody response after vaccination. Logistic regression was used for continuous variables in relation to antibody response. Of 1217 screened patients who received the hepatitis A vaccine, 40 were included, among them, 23 were male (57.5%) and 26 (65%) were African-American. Thirty-six (90%) patients had CD4 counts higher than 200 cells/mm3 . Twenty-five (62.5%) patients had an HIV-1 viral load lower than 200 copies/mL. The median age was 47 years. Half of the patients received a single dose, while the other half received a double dose of the hepatitis A vaccine. Patients were included if they completed a series of hepatitis A vaccine after having a negative hepatitis A antibody. [Table 1] outlines the results of the univariable analysis, in relation to the dependent variable (positive antibody response). Only age showed statistical significance, with younger age associated to antibody response after vaccination. In our experience, one or two doses appeared to provide comparable rates of immunogenicity. Virologic suppression and the CD4 count at the time of vaccination did not contribute to seroconversion rates. We previously observed that patients who receive a single dose even with high CD4 counts do not show higher rates of seroconversion, as with more recent studies.[3],[4] In contrast to the previous studies, we did not observe that women show higher rates of seroconversion when given standard doses of the hepatitis A vaccine and, in our cohort, half of the participants responded to vaccination.[5],[6] The main limitation of our study is the small sample size. While there may be no difference in the immune response of the HIV-positive patients who received either the single or the double dose, differences may become evident in studies with large sample size, enabling a comparison of patient groups with different CD4 counts, different contributing comorbidities, and levels of immunocompromise. Due to the small sample size, larger prospective, multi-center studies are needed to generate more reliable and convincing results.
Table 1: Demographics


Click here to view


Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.

 
   References Top

1.
Centers for Disease Control and Prevention. Prevention of hepatitis A through active or passive immunization: Recommendations of the advisory committee on immunization practices (ACIP). MMWR Recomm Rep 1999;48:1-37.  Back to cited text no. 1
    
2.
Wasley A, Samandari T, Bell BP. Incidence of hepatitis a in the United States in the era of vaccination. JAMA 2005;294:194-201.  Back to cited text no. 2
    
3.
Samandari T, Bell BP, Armstrong GL. Quantifying the impact of hepatitis A immunization in the United States, 1995-2001. Vaccine 2004;22:4342-50.  Back to cited text no. 3
    
4.
Mena G, García-Basteiro AL, Bayas JM. Hepatitis B and A vaccination in HIV-infected adults: A review. Hum Vaccin Immunother 2015;11:2582-98.  Back to cited text no. 4
    
5.
Jimenez HR, Hallit RR, Debari VA, Slim J. Hepatitis a vaccine response in HIV-infected patients: Are TWINRIX and HAVRIX interchangeable? Vaccine 2013;31:1328-33.  Back to cited text no. 5
    
6.
Czeschinski PA, Binding N, Witting U. Hepatitis A and hepatitis B vaccinations: Immunogenicity of combined vaccine and of simultaneously or separately applied single vaccines. Vaccine 2000;18:1074-80.  Back to cited text no. 6
    

Top
Correspondence Address:
Dr. Jason Dazley
Department of Infectious Diseases, New York Medical College, Saint Michael's Medical Center, Newark, NJ 07102
USA
Login to access the Email id

Source of Support: None, Conflict of Interest: None


DOI: 10.4103/0974-777X.192965

Rights and Permissions



 
 
    Tables

  [Table 1]



 

Top
  
 
  Search
 
  
    Similar in PUBMED
   Search Pubmed for
   Search in Google Scholar for
    Email Alert *
    Add to My List *
* Registration required (free)  


    References
    Article Tables

 Article Access Statistics
    Viewed2180    
    Printed22    
    Emailed0    
    PDF Downloaded20    
    Comments [Add]    

Recommend this journal

Sitemap | What's New | Feedback | Copyright and Disclaimer | Contact Us
2008 Journal of Global Infectious Diseases | Published by Wolters Kluwer - Medknow
Online since 10th December, 2008