Herpes Simplex Keratitis Clinical Trial
Official title:
A Study to Compare the Efficacy of Two Potential Diagnostic Assays: a Fluorescein Conjugated Monoclonal Antibody in Vivo Assay and Nested Real Time PCR Assay to Rapidly and Accurately Diagnose Herpes Simplex Keratitis.
The aim of this study is to compare the safety, specificity, sensitivity and ease of
procedure of two potential diagnostic assays for HSV-1 detection in the cornea. Through the
use of this new diagnostic assay, correct and early intervention would not only reduce
corneal scarring from HSK, but it would also allow the initiation of appropriate treatment
for HSV mimicking keratitis.
HSV-1 infection of the eye can result in corneal scarring and blindness. Early diagnosis of
this condition and appropriate treatment is of utmost importance. Various ocular surface
conditions can mimic herpetic keratitis in their clinical presentation and can result in
diagnostic confusion. Inappropriate or delayed treatment of herpetic corneal disease results
in increased morbidity.
In the UK at present clinical presentation is the mainstay of diagnosis. Unfortunately these
cases often present to the most inexperienced clinical staff resulting in variability in
diagnostic acumen. This often results in a delay or inappropriate diagnosis of herpetic
keratitis. Laboratory techniques presently available to aid diagnosis are infrequently used
in clinical practice. There are various reasons for their lack of use. Historically viral
culture techniques were the mainstay of investigation but were slow, requiring weeks to
provide a result. PCR is now replacing culture techniques and is relatively quick, reliable
and sensitive. Many clinicians within the UK are still not fully informed of these advances
and are therefore not utilizing these techniques to supplement clinical diagnosis.
We propose to investigate the use of topically applied fluorescent antibody against active
replicating HSV-1 in a droplet form and real time PCR detection of the virus. If successful
this should increase the potential diagnostic capabilities of GPs and other less experienced
health care workers. Such tests should reduce variability in diagnosis and the dependency on
experienced ophthalmologists to diagnose the condition.
Strategy
Patients attending the Ophthalmology departments, who fulfil the criteria as outlined below
in patient recruitment criteria, will be asked for written consent to volunteer for this
study. Tears will be removed and stored in a sterile labelled eppendorf at -70 degrees C
until further analysis. An impression cytology sample will be taken from the inflamed cornea
and stored in viral transport medium and sent to the regional virology laboratory, Belfast
for extraction and storage procedures. Blood samples will be taken and stored appropriately
until the paired 3 month samples are available for antibody testing. Monoclonal antibody
will be applied for the in vivo diagnosis of HSK as outlined below and viewed using an in
vivo confocal microscope. Photographic evidence of the result will be recorded for each
patient. Data for the nested real time PCR analysis and the monoclonal antibody test will be
recorded separately by different individuals for each patient as the study progresses.
Patient records will also be updated with the results of the tear and blood tests as the
study progresses.
Recruitment Potential:
Over 200 eye patients in the RVH Belfast, over 300 patients in Bedford and over 600 patients
in BMEC in Birmingham are treated each year with topical acyclovir for suspected HSV-1
infection. The number of patients treated within the community by GPs would significantly
increase this number. The vast majority of these patients will have never had any laboratory
confirmation of herpetic infection. The patient throughput through each hospital each year
should enable adequate recruitment to this study over the three year period. This should
ensure that the study is entirely viable from the perspective of patient numbers.
Patient numbers needed for a viable study
At present we are unable to perform statistical power calculations, as we are not aware of
the sensitivity of either of the two proposed diagnostic assays. Previous work by Kaye
SB20., et al has suggested a PCR technique with a sensitivity of 82% when used in human
corneas). In contrast, the PCR technique used here should have a much superior sensitivity
due to the use of real time analysis and the nested methodology used. These tests will be
compared against the clinical diagnosis of an experienced consultant ophthalmologist.
We accept the need for statistical power calculations in order to calculate a recruitment
level needed for a valid study. We will therefore carry out an initial study using all of
these diagnostic assays on 50 patients and the results from this will be used to perform
power calculations using the sample size method for one-sided equivalence of sensitivities
based upon McNemar s test21 to ensure adequate numbers are recruited. In addition, we hope
to over recruit (20% above this required number) to allow for patient dropout from the
study.
Patient Recruitment Criteria
Patients over the age of 16 years in which the cause of keratitis is difficult to diagnose
and in which HSK has to be excluded will be enrolled for this study. Immunosuppressed
patients including patients treated with systemic steroids will be excluded. All patients
will be asked for verbal and written consent. All patients will continue to be followed
according to clinical requirements. In addition to routine assessment additional clinical
categorisation by the attending consultants into those patients thought to (a) have, and (b)
not have, clinical evidence in keeping with herpetic infection will be recorded.
In vivo immunofluorescence diagnostic procedure
30 microlitres of fluorescent-labelled mAB (2mg/ml), (same mAB as used in the previous study
by Sharma A., et al7) in normal saline solution will be applied to the eye. After 20 minutes
unbound antibody will be rinsed away with saline solution. The eye will be viewed with a
slit lamp or an in vivo confocal microscope if available. mAB penetration through the layers
of the cornea will be recorded. In addition, evidence of stromal inflammation will be
recorded and its relationship to specific fluorescence noted. This will indicate the
contribution of active herpetic infection (by specific fluorescence in either epithelium,
stroma or both) as a causative effect rather than an immunological response to latent virus.
Comparison of in vivo results with nested real time PCR technique
Impression cytology will be carried out, prior to the application of the antibody, to
confirm the presence/absence of viral antigens using nested real time PCR analysis. The
potential for amplicon contamination associated with nucleic acid amplification test use is
well recognised and makes mandatory the use of (a) separate, designated work stations and
(b) a uni-directional work-flow from specimen preparation to amplified product analysis;
this model of operation is standard in the regional virology laboratory. All PCR experiments
will therefore be carried out under the supervision of Dr. Hugh O'Neill in the Regional
Virology Laboratory, RVH, Belfast.
Impression cytology samples will be sent to the laboratory in viral transport medium. Each
specimen will be vortexed for 15 seconds on receipt in the laboratory to resuspend the
cellular content. A volume will be removed for PCR and the remainder will be stored.
Nested PCR will be undertaken using primers recognising the HSV-1 gpD gene (HSV-1 outer
products will be 221 and 184 base pairs (bp) while the inner products will be 138 and 101 bp
respectively). Hot-start PCR will be performed in a Perkin Elmer GeneAmp 2400 thermal cycler
with 10 μl specimen plus 40 μl of mix and subjected to 35 first round cycles. One microlitre
of product will be transferred to 49μl of second round mix for 25 second round cycles.
Impression cytology samples taken from non-inflamed eyes from recruits with no history of
herpetic eye infection will be used as known negative samples. A positive HSV control and a
distilled water negative control will also be included in each run. First and second round
products will be visualised together on ethidium bromide-stained 2% agarose gels and
photographed (Polaroid). Appropriately sized bands present on second round only, or present
on both first and second rounds, will be recorded as positive and strong positive
respectively. All positive specimens will be re-tested.
Laboratory staff responsible for the PCR test will not be aware of the results from the in
vivo antibody test. Comparison will be made between the sensitivity and specificity of the
monoclonal antibody in vivo assay and the nested real time PCR diagnosis.
Investigating the effect of mAB on the ocular surface inflammatory milieu Analysis of the
general cytokine profile will also be assessed by monitoring the cytokine profile of tears
at two different time points: prior to monoclonal antibody treatment and again 30 minutes
after the application of the antibody. Cytokine profile of tears will be analysed using
proteomics with a protein biochip (RANDOX Labs. Ltd.) capable of simultaneous quantitative
detection of an array of pro- and anti- inflammatory cytokines. Tear samples from patients
suspected of active herpetic infection but who have not received antibody will serve as
controls. Such analysis will allow statements to be made regarding the potential
inflammatory/immunological reaction to the monoclonal antibody.
Investigating a potential systemic immunological reaction the mouse mAB Ten millilitres of
clotted blood will be taken prior to the application of the monoclonal antibody to test for
the presence of pre-existing antibody. In addition, at the 3 month check up a further 10
millilitres of blood will be taken and analysed again for antibodies which may have formed
in the three month interface after the application of the monoclonal to the cornea.
The avascular cornea is thought to be an immunologically privileged site, making the
potential of an immune response to the antibody less likely.
;
Time Perspective: Prospective
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Terminated |
NCT02045082 -
The Flocked Swab and the Traditional Fiber Swab for the Diagnosis of the Herpes Simplex Epithelial Keratitis
|
Phase 4 | |
| Recruiting |
NCT03217474 -
Femtosecond Laser-assisted Corneal Debridement for Herpes Simplex Keratitis
|
N/A |