1. Liquid based cytology
Liquid based Cytology

2. Background
The conventional pap smear has been the most successful screening test
Screening every 3-5years has resulted in a 70% reduction in incidence

3. Why LBC (Liquid based cytology) has been introduced ?
Continuing improvement to the Cervical screening Programme
Limitations of conventional cytology
Modernisation of the technique
Future benefits
Extra tests – HPV, chlamydia, Neiseria Gonorrhoea.

4. Limitations Of Conventional Smear (From UK studies)
False Negative Rate of up to 55%1
Sampling and interpretive errors
Ambiguous reports of 6.4%2
70% are truly negative
30% represent more severe abnormality
Inadequate specimens of 9.7% 2
1. Hutchinson et al., AJCP, Vol 101-2; , 2. DOH Statistical Bulletin 2000/2001

5. Sources Of False Negatives
Sampling issues (70%)
cells not collected on the sampling device
cells collected, but not transferred to the slide
Thicker and thinner areas
Nuclear feathering artifact
Interpretive issues (30%)
abnormal cells present on slide but either not seen or misinterpreted
Blood/mucus
Air drying artifact
Blood mucus overlap not preserved well

6. What does 'Liquid Based Cytology' mean?
Literally it means
“cytology (the study of cells) through a liquid medium.”

7. Liquid-based cytology techniques
he TransCyt® filter has been plunged into the sample, it rotates at a high speed and facilitates cell and mucus dispersion. A vacuum is then applied to the filter, which collects cells on a 5 μm porosity membrane. A software program allows a homogeneous deposition of cells until saturation. The TransCyt filter is then inverted and a positive pressure allows cells to adhere to an electronegative slide. After insertion of another TransCyt filter and of another slide, the whole procedure may be repeated until the entire sample has been treated.

8. Technique of LBC Step : I Collection of sample

11. Specimen Collection PreservCyt Solution.
Capped, labeled, and sent to the laboratory equipped with a ThinPrep 2000 Processor .
Composition
Buffered methanol
No active ingredient
Storage
15 to 30 C for 6 weeks

12. Thinprep Processor
Cell dispersion
Cell Collection
Cell Transfer

13. Thin Prep processor (1)Cell dispersion
Swirling the sampling device in the preservation solution
Strong enough to separate debris and disperse mucus, but gentle enough to have no adverse effect on cell appearance.

14. Thin Prep processor (2) Cell Collection
A gentle vacuum is created within the ThinPrep Pap Test Filter, which collects cells on the exterior surface of the membrane.
Cell collection is controlled by the ThinPrep 2000 Processor’s software that monitors the rate of flow through the ThinPrep Pap Test Filter.

15. Thin Prep processor (3) Cell Transfer
After the cells are collected on the membrane, the ThinPrep Pap Test Filter is inverted and gently pressed against the ThinPrep Microscope Slide.
Natural attraction and slight positive air pressure cause the cells to adhere to the ThinPrep Microscope Slide resulting in an even distribution of cells in a defined circular area.

16. Summary

17. Advantages of LBC

21. Conventional smear Conventional Pap Smear (Macroscopic)
• The manual smearing method is readily noted macroscopically. Conventional slide experience is transferable to the ThinPrep process. Cytology does not have to be relearned, base knowledge is merely refined.

22. The prepared slide with the new ThinPrep
TP (Macroscopic)
• The key difference in presentation is no longer seeing the smear pattern. ThinPrep takes the same material which is concentrated onto the center of the slide in a thin, uniform layer. Specimen preparation is standardized, eliminating the inconsistency associated with manual preparations.
The prepared slide with the new ThinPrep

23. What we see under the microscope conventional smearCP
• Microscopically, the uneven distribution of cellular material associated with the CP smear pattern is evident.

24. TP
Same Patient
• Tissue architecture is maintained. TP rearranges the relationship of cell groups on the glass slide. A group/sheet of endocervical cells present represents this.
What we see under the microscope. Notice the clean back ground and how well the cells are dispersed rendering easier to interpretation.

28. Disadvantages of LBC

29. Disadvantages of LBC

31. Manual membrane based method of LBC
Relatively inexpensive method
Equipments required- vortexer and laboratory centrifuge

32. Solution required are;
Fixative solution
Surepath preservation fluid
Lab prepared- water, NaCl, Na Citrate, 10% formalin,alcohol
Polymer solution
Agarose, polyethylene glycol
Alcohol, poly-L-lysene

33. Procedure Collection of sample Specimen is vortex mixed
Centrifuge at 800 g for 10 min
Vortex mix
Add 1-2 ml of polymer solution to tube
Decant fixative and blot excessive fixative
Allow 3-6 drops of suspension to glass slide
Allow to dry
Stain with conv. Pap

34. Laser Scanning Cytometry

35. What is the need?
Our limited ability to undertake accurate, quantitative measurement of cellular and subcellular factors
Established technologies in clinical pathology, including conventional microscope-based histopathology and histochemistry, fluorescence microscopy, flow cytometry and computer-based image cytometry, all have limitations.

36. Introduction Imaging + cytometric analysis
Not random, but event-based.
It is closely related to conventional flow cytometry, which also analyzes individual cells that meet certain characteristics (and is also event-based). Both are therefore cytometric techniques
Image or scanning cytometry (IC) combines imaging and cytometric analysis in a single technology platform.
Rather than randomly imaging an entire field (like a microscope does), it selects, images and measures cells that meet certain user-adjustable criterion (such as size or fluorescence). It is therefore not random, but event-based.
It is closely related to conventional flow cytometry, which also analyzes individual cells that meet certain characteristics (and is also event-based). Both are therefore cytometric techniques Unlike conventional flow cytometry, IC usually analyzes cells fixed to a horizontal surface. However, the technology (light sources,
detectors, etc.) is very analogous to traditional flow cytometry. With scanning cytometry, imagery becomes a parameter, and relates to the other parameters (scatter and fluorescence).

37. Limitations of Flow cytometry
time-resolved events such as enzyme kinetics cannot be analyzed.
Simultaneous study of Morphology of the measured cell is not possible.
Cell analysis is at zero spatial resolution.
The cell once measured cannot be re-analyzed with another probe(s)

38. 5. Analysis of solid tissue requires cell or nucleus isolation, a procedure that may produce artifacts and loss of the information on tissue architecture. 6.size samples such as fine needle aspirates, spinal fluid, thus, are seldom analyzed by FC. 7. The measured sample cannot be stored for archival preservation.

39. Introduction 2 manufacturers:
CompuCyte Corp. (Cambridge, MA)
Olympus Optical Co. (Tokyo), offers many advantages of flow cytometry but has no limitations listed above.
The analytical capabilities of LSC, therefore, complement these of FC, and extend the use of cytometry in many applications

41. Principle

42. Lasers Lasers Photomultipliers
The microscope (Olympus Optical Co.) is the key part of the instrument, and it provides
essential structural and optical components (Fig. 1). The specimen deposited on a micro-scope slide on the stage of the microscope is illuminated by laser beams that rapidly scan the slide. The beams from two lasers (argon ion and helium-neon) spatially merged by dichroic mirrors are directed onto the computer controlled oscillating (350 Hz) mirror, which reflects them through the epi-illumination port of the microscope and images through the objective lens onto the slide. The mirror oscillations cause the laser beams to sweep the area of micro-scope slide under the lens. The beam spot size varies depending on the lens magnification, from 2.5 (at 40x) to 10.0 m (at 10x). The slide, with its xy position monitored by sensors, is placed on the computer-controlled motorized microscope stage, which moves at 0.5 m steps per each laser scan, perpendicularly to the scan. Laser light scattered by the cells is imaged by the condenser lens and its intensity recorded by sensors. The specimen-emitted fluorescence is collected by the objective lens and part of it is directed to a charge-coupling device(CCD) camera for imaging. Another part is directed to the scanning mirror. Upon reflection,it passes through a series of dichroic mirrors and optical emission filters to reach one of the four photomultipliers. Each photomultipler records fluorescence at a specific wavelength range, defined by the combination of filters and dichroic mirrors. A light source, additional to the lasers, provides transmitted illumination to visualize the objects through an eyepiece or the CCD camera.
Photomultipliers

44. Interpretation

45. Thresholding on flow cytometer
Setting the threshold (or discrimination) on the flow cytometer allows us to eliminate unwanted cells (like erythrocytes) from the saved analysis

46. Thresholding (or contouring) on the laser scanning cytometer
On the laser scanning cytometer, any event that is above the threshold (usually DNA fluorescence or sometimes forward scatter) is also considered a “cell” and is also displayed for all parameters.
The instrument marks such
events with a red “contour”,
which contains the amount
of fluorescent signal above
the threshold.
Thresholding on the LSC is
therefore referred to as
“contouring”

47. Event-based contouring on the iCys
The red region is the event or thresholding contour. It is analogous to “thresholding” or “discrimination” on the flow cytometer. It defines the minimum signal intensity that defines a cell. Everything else below it is ignored. Like in cytometry, you need a universal parameter (like scatter or DNA luorescence) as the trigger for threshold contouring
The green region is the inte grating contour. You can set this any number of pixels out from the thresholding contour and measure the brightest pixel (Max Pixel), or the total fluorescence (Integral) within the green region.
The blue regions are the background contours. You can also set these any number of pixels out from the integrating contour, away from the cell. The signal between them is interpreted as the autofluorescence background, which is subtracted from the other signals.

49. Parameters studied by LSC
Integrated fluorescence intensity
The maximal intensity
The Integration area
The perimeter of the integration contour (in micrometers).
The fluorescence intensity integrated over the area of a torus of desired width defined by the peripheral contour located around (outside) of the primary integration contour.
1. Integrated fluorescence intensity representing the sum of intensities of all pixels (pic-ture elements) within the integration contour area. The latter may be adjusted to a de-sired width with respect to the threshold contour (Fig. 2).
2. The maximal intensity of an individual pixel within this area (maximal pixel).
3. The integration area, representing the number of pixels within the integration contour.
4. The perimeter of the integration contour (in micrometers).
5. The fluorescence intensity integrated over the area of a torus of desired width defined
by the peripheral contour located around (outside) of the primary integration contour.
For example, if the integration contour is set for the nucleus, based on red fluorescence
(DNA stained by propidium iodide, PI), then the integrated (or maximal pixel) green
fluorescence of FITC (fluorescein isothiocyanate)-stained cytoplasm can be measured
separately, within the integration contour (i.e., over the nucleus) and within the periph-
eral contour (i.e., over the rim of cytoplasm of desired width outside the nucleus). All
above values of fluorescence (1,2,4) are automatically corrected for background,
which is measured outside the cell, within the background contour (Fig. 2).
6. The Xy coordinates of maximal pixel locating the measured object on of the microscope
stage. 7. The computer clock time at the moment of measurement.
The measurements by LSC are relatively rapid; having optimal cell density on the slide up
to 5000 cells can be measured per minute. The accuracy and sensitivity of cell fluorescence measurements by LSC are comparable to the advanced flow cytometers

50. 6. The X-Y coordinates of maximal pixel locating the measured object on of the microscope stage. 7. The computer clock time at the moment of measurement.

51. Applications in Cytology and Pathology

52. In Cytology It negates disadvantages of Flow cytmetry Image analysis
Requires sufficient amount
Verification /reproducibility not possible
Not for adherent cells
Flow cytmetry
Experience of cytologist needed
Image analysis

53. Circulating tumor cells
Quantification monitoring for potential metastasis/recurrence
Molecular studies therapeutic purposes

54. Apoptosis studies
Characterized by certain morphological features e.g. nuclear fragmentation, nuclear condensation
Methods e.g. annexin V, loss of transmembrane potential in mitochondria, analysis of nuclear fragmentation, alteration of DNA condensation.
Intensity of maximal pixel of fluorescence is a sensitive marker of local hypo- or hyper-chromicity within the cell, reflecting low or high concentration (density) of the fluorescent probe. One of the early applications of LSC along this line was to detect chromatin conden-sation. Namely, DNA in condensed chromatin, such as mitotic or apoptotic cells, shows in-creased stainability (per unit area of chromatin image) with most fluorochromes. Thus, even
when integrated fluorescence of the analyzed cells (representing their DNA content) is the same, the intensity of maximal pixel of the cell with condensed chromatin is higher than that of the cell with more diffuse chromatin structure. Maximal pixel of the DNA-associated fluorescence was used as a marker to distinguish mitotic and immediately post-mitotic G 1 cells from interphase cells [5,6]. Although mitotic cells can be recognized by FC using a variety of markers [reviewed in 7], the advantage of this approach by LSC is that a single fluorochrome
is used to discriminate between G 1 vs S vs G 2 vs M phase cells.

56. Immunophenotyping of leucocyte
Especially useful when amount of obtained sample is minimum e.g. neonate, critically ill patients
Upto 5 flurochromes in < 15 microlit of peripheral blood.
Analysis by 2 methods
Specific Immunostaining e.g. CD45
DNA staining with 7-AAD- difference in intensity with different leucocytes

58. Ploidy and DNA index
Anueploid number characteristic of a malignant cell e.g. Gastric, colon, kidney, head and neck etc.
Prognostic marker in several tumors
LSC measures amount of DNA in cell

59. Tumor cells are identified and gated based upon cytokeratin staining.
To verify the morphology of the two populations, cells can be restained with Wright-Giemsa or H & E. Cells from each region can be relocated and visualized by the CompuSort™ process.

60. Bacterial detection detect live and dead bacteria,
estimate cell numbers, and
calculate live/dead ratios.
The methods are easier and more accurate than traditional, manual counts.
propidium iodide (PI), unable to permeate the intact cell membrane of a living cell, but does label dead cells with red fluorescence. SYTO® 16(Molecular Probes) will label the nucleic acids of living cells with green fluorescence. Shown here are E. coli bacteria captured on a membrane and stained with PI and SYTO 16

61. Disadvantages Expensive instrumentation
Exact DNA content of paraffin block is difficult to determine.

62. Thank You