CD4
Measurements in Patients with HIV: Are They Feasible for Poor
Settings?
Zvi
Bentwich
Zvi
Bentwich is Professor of Medicine (Emeritus), Hebrew University
Medical School, Professor in the Department of Microbiology
and Immunology, Ben Gurion University Health Sciences Faculty,
Beer Sheba, and Chief Scientist, Rosetta Genomics, Rehovot,
Israel. E-mail: zbentwich@rosettagenomics.com
Competing
Interests: The author declares that he has no competing
interests. Rosetta Genomics has not developed any devices for
HIV evaluation in resource-poor settings.
Published:
July 19, 2005
DOI:
10.1371/journal.pmed.0020214
Copyright:
© 2005 Zvi Bentwich. This is an open-access article distributed
under the terms of the Creative Commons Attribution License,
which permits unrestricted use, distribution, and reproduction
in any medium, provided the original work is properly cited.
Abbreviation:
ART, antiretroviral therapy
Citation:
Bentwich Z (2005) CD4 Measurements in Patients with HIV: Are
They Feasible for Poor Settings? PLoS Med 2(7): e214
Measurement
of peripheral blood CD4 T lymphocytes is probably the most important
laboratory assay for evaluation and monitoring of patients with
HIV. The CD4 count is critical for determining the clinical
stage of HIV infection, for deciding when to start antiretroviral
therapy (ART), for evaluating the efficacy of treatment, and
for changing the medications when necessary. Most HIV treatment
decisions are therefore based upon the CD4 count [1–3].
Flow Cytometry
The most
common technique for measuring CD4 counts in developed country
settings is flow cytometry. Flow cytometers use lasers to excite
fluorescent antibody probes specific for various cell surface
markers, such as CD3, CD4, and CD8, which distinguish one type
of lymphocyte from another.
As Rodriguez
et al. point out in their study in this issue of PLoS Medicine
[4], the cost of a flow cytometer ranges
from $30,000 to $150,000, and the reagents needed for determining
the lymphocyte surface markers by this method are very costly.
In addition, use of flow cytometry requires technical and operational
expertise as well as a reliable electricity source. Considering
all these factors together, it is no surprise that CD4 measurements
cannot be widely applied in developing world settings.
Why CD4 Counts Matter
in Developing Countries
This grim
reality—the lack of facilities to measure CD4 counts in poor
countries—stands in sharp contrast to the urgent need for instituting
rational and effective ART in these countries. The absence of
tools to measure CD4 counts clearly jeopardizes the success
of the recently launched global campaigns to fight AIDS, such
as those of the World Health Organization and the Global Fund
to Fight AIDS, Tuberculosis, and Malaria. These campaigns aim
to distribute ART to millions of people with HIV, mostly living
in developing countries. Regretfully, it is highly likely that
these major efforts will fail, unless improved and widely used
means for counting CD4 cells become available and can be applied
where they are most needed. Since at least 35 million people
are infected with HIV, and several million of them are in need
of urgent lifesaving ART, the issue of CD4 monitoring has become
a crucial one.
Rodriguez
et al. point out that several efforts have been made to develop
alternative, affordable CD4 counting methods for resource-poor
settings [4]. These include improved flow cytometric
approaches and microbead capture/separation of CD4 cells followed
by manual cell counting [5–8]. Also, new single-purpose flow
cytometers have been designed that perform the test at a much
lower price. Though all these assays are indeed cheaper than
regular flow cytometry, they suffer from decreased accuracy
and, most importantly, they are all of low throughput.
A New Method for
Counting CD4
Rodriguez
et al. describe a novel method for counting CD4 in resource-poor
settings (Figure 1) [4]. The method is based on a novel microchip
detection system for measuring various analytes in very small
volumes. A series of chemical and immunological reactions carried
out on microspheres are visualized and captured on a charge-coupled
device (developed for digital camera technology). This method
allows for accurate measurement of CD4, CD8, and CD4/CD8. The
prototype used for demonstration of the new apparatus shows
extremely good agreement with currently used flow cytometry.
Most importantly, the investigators claim that the cost of each
assay is much lower than that for flow cytometry.
There are,
however, a number of unresolved issues in this study that need
further clarification before the assay can meet the expectations
for becoming a widely used tool in resource-poor settings. Firstly,
the study was performed with a prototype apparatus, tailored
to meet the requirements of the study, but not yet representing
a commercially established and viable production line. Secondly,
though the authors state that the price of each CD4 determination
will become much cheaper, it is not clear how much each assay
will cost in the end, and whether the final cost is realistic
in the context of developing countries. It is clear, though,
that the actual price of the assay will change once it is widely
and consistently used on a large scale. Thirdly, although a
few children were tested (six infants in total), the results
in this small group remain questionable, and therefore the application
of the test to pediatric populations needs further testing.
It may well be that application to pediatric patients will require
an improved apparatus or improved handling.
Conclusion
Despite
these reservations, the authors of this study should be commended
for addressing an extremely important issue and developing this
novel approach for counting CD4 in patients with HIV. Their
study may lead to further development of such an apparatus,
which is sorely needed for the global fight against AIDS. Such
efforts will hopefully be noticed by public funding agencies,
leading to the improvement of tools for measuring CD4 counts.
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