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Hyposplenic patients are at risk of overwhelming post-splenectomy infection (OPSI), which carries mortality of up to 70%. Therefore, preventive measures are warranted. However, patients with diminished splenic function are difficult to identify. In this review we discuss immunological, haematological and scintigraphic parameters that can be used to measure splenic function. IgM memory B cells are a potential parameter for assessing splenic function; however, more studies are necessary for its validation. Detection of Howell–Jolly bodies does not reflect splenic function accurately, whereas determining the percentage of pitted erythrocytes is a well-evaluated method and seems a good first-line investigation for assessing splenic function. When assessing spleen function, 99mTc-labelled, heat-altered, autologous erythrocyte scintigraphy with multimodality single photon emission computed tomography (SPECT)-CT technology is the best approach, as all facets of splenic function are evaluated. In conclusion, although scintigraphic methods are most reliable, they are not suitable for screening large populations. We therefore recommend using the percentage of pitted erythrocytes, albeit suboptimal, as a first-line investigation and subsequently confirming abnormal readings by means of scintigraphy. More studies evaluating the value of potentially new markers are needed.
The spleen is the largest lymphoid organ in the human body. Its rich and diverse population of immune cells and its ingenious anatomy that enables optimal surveillance and phagocytosis of circulating blood elements play an important role in the defence against pathogens. Table 1 summarizes the different aspects of splenic functions. After splenectomy, patients are at increased risk of overwhelming post-splenectomy infection (OPSI; see Table 2 [1–4].
Apart from patients with a status after splenectomy, there is a much larger group of patients with diminished splenic function. Many diseases are associated with a dysfunctional spleen (Table 3) and the degree of splenic dysfunction varies between patients . For patients suspected to have a spleen with diminished function, it is important to quantify their splenic function in order to assess the risk of developing OPSI. Subsequently, preventive measurements can be taken and, in the case of infection, therapy can be started without delay. In this review we evaluate the methods available to measure splenic function.
Throughout the years, several methods have been developed to quantify the many different functions of the spleen. These methods are based on haematological, immunological and scintigraphic parameters.
Haematological methods reflect the capacity of the spleen to phagocytose deviant erythrocytes and to facilitate an environment wherein erythrocytes rid themselves of solid waste material [14, 15]. In the event of splenic dysfunction these capacities are impaired, which results in an increase in abnormal circulating red blood cells. Furthermore, large amounts of thrombocytes and leukocytes normally reside in the spleen. Circulating thrombocyte- and leukocyte counts can either be increased or decreased, indicative of hyposplenism in a patient with a dysfunctional spleen (for example, thrombocytosis in asplenia and thrombopaenia associated with splenomegaly) [13, 16].
One of the first methods available to evaluate splenic function was the detection of erythrocytes containing Howell–Jolly bodies, using a light microscope viewing a stained peripheral blood smear [17, 18]. Howell–Jolly bodies are basophilic DNA remains from the nucleus of the erythrocyte precursor cell. Normally, upon leaving the bone marrow, the erythrocyte precursor cell expels its nucleus. In some erythrocytes, however, a small portion of DNA remains. Normally, the spleen clears the erythrocyte of these nuclear remnants or removes the erythrocytes from the circulation, but when the spleen is absent or has a decreased function, these Howell–Jolly body-containing erythrocytes remain in the circulation. A recently developed method uses flow cytometry to quantify the amount of erythrocytes containing Howell–Jolly bodies .
Other abnormalities that can be seen on peripheral blood smears of patients with absent or diminished splenic function are acanthocytes (spur cells), target cells (codocytes: erythrocytes with a pattern of central staining, a ring of pallor and an outer ring of staining), haemoglobin remnants (Heinz bodies), siderocytes and iron granulocytes (Pappenheimer bodies) [13, 16] .
In individuals with a dysfunctional or absent spleen the membrane of erythrocytes appears to contain so called “pits” when studied with interference phase microscopy . With electron microscopy it was shown that these “pits” are in fact large vacuoles (about 300 nm in diameter) beneath or attached to the plasma membrane. These vacuoles have low optical density, because of waste material contained in the erythrocyte, such as ferritine, haemoglobin and rest material of mitochondria and membranes [14, 15, 21]. In case of normal splenic function, pits are seen in 0–4% of the erythrocytes [20, 22, 23]. A pit count above 4% has been associated with hyposplenism, although asplenia or clinically relevant hyposplenism is most often associated with much higher values, ranging from 15 to 70% [22, 24, 25]. Casper et al. noted that in 5 patients with sickle cell disease who developed sepsis and/or meningitis, pit counts were higher than 15% and therefore the authors suggested this as a cut-off value for significant splenic dysfunction . The same cut-off value was suggested by Corazza et al., who noted that patients who underwent splenectomy had functional residual splenic tissue when pits counts were beneath 16% .
Another method of evaluating spleen function is counting erythrocytes containing argyrophilic inclusions, where normal values range from 0 to 3%. This method uses a silver stain and in comparison with a normal Wrights stain, the argyrophilic inclusions are shown to be Howell–Jolly bodies, Pappenheimer bodies and other inclusions visible in patients with a decreased or absent splenic function .
The spleen contains a large amount of immune cells . In comparison to the peripheral blood lymphocyte compartment, the spleen percentually contains more B-cells and less CD4+ and CD8+ T cells. The percentage of CD8+ T cells is higher in the spleen, leading to an inverse CD4/CD8 ratio. Both splenic CD4+ and CD8+ T cell populations show a higher number of activated cells and splenic CD8+ T cells show a more differentiated cytotoxic CD27-CD45RA+ memory phenotype. Thus, the distribution of the different lymphocyte subsets is markedly different between spleen and peripheral blood, inferring an important and distinct role for the spleen in CD4+ and CD8+ T cell activation . After splenectomy, some immunological functions of the spleen can be taken over by other organs, such as the liver, bone marrow and peripheral lymph nodes. Therefore, these functions are not suitable as a reliable parameter for measuring spleen function. However, the spleen plays a specific role in the defence against encapsulated bacteria [1–4]. This is mainly related to the marginal zone (MZ) containing marginal zone B cells (MZ B cells) and macrophages. Marginal zone macrophages are able to capture whole encapsulated bacteria from the circulation and subsequently initiate a humoral immune response . MZ B cells are a distinct B cell lineage that, unlike other B cell lineages, develop and mutate immunoglobin (Ig) receptors during the first years of life without being engaged in any immune response. Upon stimulation with thymus-independent type 2 (TI-2) antigens expressed by encapsulated bacteria, the prediversified MZ B cells can rapidly proliferate and differentiate into antigen-presenting cells or into IgM-, IgG-, and IgA-secreting plasma cells, circulating for several months. MZ B cells do not differentiate into memory cells and are therefore part of the (immediate) innate immunity against invading pathogens [31–33].
Marginal zone B cells do not only reside in the MZ, but are also present in the circulation and in other lymphoid tissue [34–36]. The spleen is, however, essential for the maintenance of the MZ B cell population, as appears from a decrease in MZ B cell counts after splenectomy. In contrast to one report , other studies have shown that young patients with congenital asplenia have a normal blood MZ B cell population, whereas this circulating MZ B cell subset fails to expand in older asplenic individuals [32, 37]. Therefore, the amount of circulating MZ B cells may be an indication of immunological function of the spleen. The effect of diminished spleen function on the composition of naïve, memory and effector (antigen-specific) T cells in the circulation is not yet known. Decreased numbers of circulating memory B cells have been described in patients with diminished splenic function [31, 32, 37], although this might be due to a decrease only in IgM memory B cells rather than in other B memory cells [31, 37].
Some studies have described tuftsin as a potential marker for immunological spleen function, since production of this peptide is mainly dependent on the spleen [38, 39]. Tuftsin is a tetrapeptide with protective bactericidal characteristics, as it has been shown to stimulate phagocytosis by neutrophils and macrophages . Decreased serum levels of tuftsin are seen in splenectomised patients [38, 39] and in patients suffering from sickle cell disease  and coeliac disease .
Like haematological parameters, scintigraphic parameters use the capacity of the spleen to filter the blood of deviant cells and particles to measure its activity. The radiopharmaceutical most commonly used for this purpose is technetium-99m (99mTc)-labelled, heat-altered, autologous erythrocytes, which have replaced the previously commonly used 99mTc-labelled sulphur colloids [43–48]. 99mTc-labelled sulphur colloid scintigraphy has been used for visualisation of the phagocytic function of the liver and spleen and was once a common study for evaluating for the presence or absence of neoplastic disease, cirrhosis or portal hypertension, being largely supplanted by other modalities like ultrasonography, (PET)-CT or MRI to date . For the assessment of spleen function or the presence of an accessory spleen, 99mTc-labelled, heat-altered, autologous erythrocyte scintigraphy is now recommended, because, in contrast to sulphur colloid scintigraphy, sensitivity is not hampered by the relatively high liver uptake [43–48, 50]. Sulphur colloids are captured by phagocytosis, whereas autologous, heat-altered erythrocytes are sequestrated by the normal spleen [50, 51]. The normal spleen accumulates about 90% of injected autologous, heat-altered erythrocytes, in contract to 10% of injected sulphur colloids, which are mainly phagocytosed by the liver . After intravenous re-injection of these cells, splenic function can be determined by:
Besides quantitative information on splenic function, planar or dynamic scintigraphy enables visualisation of organ function. In addition to planar scintigraphy, modern multimodality single photon emission computed tomography (SPECT)-CT gamma cameras enable assessment of both function and anatomy (organ volume and structure) within a single investigation, potentially introducing clinically useful parameters like organ-specific functional volumes .
Alternatively, unaltered autologous or donor erythrocytes or platelets can be radio-labelled for assessment of pathological sequestration in the spleen in patients with low peripheral cell counts, such as in idiopathic thrombocytopaenic purpura or auto-immune anaemia [43, 50, 53–55]
As there are many approaches to assessing splenic function, the question arises as to which method is most reliable and which is best for clinical use. Knowledge about correlation and functionality of the different available methods is required before a deliberate decision on which method to use can be made. In the next few paragraphs we give an overview of studies comparing the haematological, immunological and scintigraphic parameters in the measurement of splenic function.
Although 99mTc-labelled, heat-altered, autologous erythrocytes as well as 99mTc-labelled sulphur colloids have been used in studies on splenic function, not much recent data can be found on their correlation when determining the amount of functional splenic tissue. When computing splenic volumes based on planar scintigraphy in two groups of coeliac patients, splenic volumes derived from 99mTc-labelled sulphur colloid scintigraphy correlated well with those from 99mTc-labelled, heat-altered erythrocyte scintigraphy . Furthermore, there was a good correlation between volume of functional splenic tissue and splenic function measured using 99mTc-labelled heat-altered erythrocyte clearance rates from the circulation. Another publication by Smart et al. in patients with mainly inflammatory bowel disease (IBD) showed a strong correlation between clearance of the cells from the circulation and functional spleen volume, with a large variation around the regression line, leading to the conclusion that functional spleen size determination was not able to replace measurement of the rate of heat-altered erythrocyte clearance from the circulation in the assessment of hyposplenism . However, these studies were performed in the pre-tomographic and ultrasonographic era using planar imaging for volume calculation, making it less reliable. Furthermore, only functioning spleen was visualised and eligible for volume calculation, implying a direct correlation between function and size [57, 58]
A more recent study by Gotthardt et al. showed that spleen–liver ratios as soon as 10 min after reinjection of 99mTc-labelled, heat-altered erythrocytes reliably predict spleen function in IBD patients when compared to the rate of clearance of the cells from the circulation. The spleen–liver ratio measured with 99mTc-labelled sulphur colloids showed no correlation with the clearance of the 99mTc-labelled, heat-altered erythrocytes .
The correlation between haematological parameters and scintigraphic parameters has been studied more accurately. In patients with sickle cell disease (SCD), a correlation was found between the uptake of 99mTc-labelled sulphur colloid by functional splenic tissue and the percentage of pitted erythrocytes [23–25]. In a study by Pearson et al. amongst 64 children with homozygous SCD between 8 and 13 months of age, it was found that sensitivity, specificity and predictive values were all between 90% and 98% when correlating uptake with a percentage of pitted erythrocytes of less than 3.5% . Another study by Lane et al. described patients with heterozygous SCD (HbSC), where it was demonstrated that pit counts of more than 20% were indicative of functional asplenia, whereas pit counts lower than 20% were associated with normal or near normal splenic function . Furthermore, in a study of patients with coeliac disease and dermatitis herpetiformis, a correlation was found between the percentage of pitted erythrocytes and the size of functioning splenic tissue, as measured by using 99mTc-labelled, autologous, heat-altered erythrocytes rather than sulphur colloids . In this same group of patients, a significant correlation was found between the percentage of pitted erythrocytes and the clearance rate of 99mTc-labelled, heat-altered erythrocytes. However, another study describing patients with megaloblastic anaemia and iron-deficient anaemia, which are rare causes of hyposplenia, no correlation was found between the percentages of pitted erythrocytes and the blood clearance rate, splenic uptake values and splenic volumes . An explanation for these results could not be given by the authors; however, they state that erythrocyte pits may be heterogeneous in origin, composition, or removal kinetics and may be different in individuals who are hyposplenic for various reasons.
The presence of the Howell–Jolly bodies has historically been associated with diminished splenic function. However, Howell–Jolly bodies have been shown not to correlate with blood clearance of the 99mTc-labelled, heat-altered erythrocytes [58, 59]. Similar results were obtained using 51chromium-labelled heat-altered erythrocytes . The presence of Howell–Jolly bodies did also not correlate with the spleen–liver activity ratio measured with either 99mTc-labelled, heat-altered erythrocytes or 99mTc-labelled sulphur colloids .
Although there is discussion in the literature, it was found that the percentage of erythrocytes containing Howell–Jolly bodies correlated with the percentage of pitted erythrocytes [23, 62]. This correlation, however, was only present at pit counts higher than 8% and when at least 10,000 erythrocytes were examined. Mild cases of hyposplenism could not be detected by determining percentages of erythrocytes with Howell–Jolly bodies, since a pit count above 4% is indicative of hyposplenism. No note was made of what percentage of erythrocytes containing Howell–Jolly bodies indicates hyposplenism .
The argyrophilic inclusion-positive erythrocyte count has sensitivity of 88.9% and specificity of 97.1% for splenic dysfunction when using the percentage of pitted erythrocytes as a gold standard .
Because the amount of circulating IgM memory B cells was first described in 2005 as a method of quantifying splenic hypofunction, research on this subject is still limited. Two studies describe a correlation between the amount of circulating IgM memory B cells and the percentage of pitted erythrocytes in treated patients with coeliac disease and IBD [37, 63]. In one study, patients with IBD were divided into either having a decreased splenic function (>4% pitted erythrocytes) or having a normal splenic function (<4% pitted erythrocytes) and both were compared with a control group . Patients with decreased splenic function were shown to have lower amounts of circulating memory B cells, mainly IgM memory B cells, compared with healthy controls as well as individuals classified as having normal splenic function. Furthermore, IgM memory B cells were shown to be completely absent in the peripheral blood of splenectomised patients. As described above, serum tuftsin might be indicative of splenic function, although not much research on the subject has been published. This potential marker was studied in 52 untreated patients with coeliac disease . In accordance with the study on IgM memory B cells, patients were divided into groups based on pit count. It was found that hyposplenic as well as eusplenic coeliac patients had significantly lower tuftsin activity than healthy controls, but significantly higher than splenectomised patients. There was less tuftsin activity in hyposplenic patients than in eusplenic patients. Furthermore, a correlation was found between serum tuftsin activity and the percentage of pitted erythrocytes.
Knowledge about splenic function is important, since patients with an absent spleen or decreased splenic function are at risk of developing severe infections with a high mortality rate. Quantification of spleen function could become an important tool for physicians in their decision-making regarding the need for preventive measures. However, when assessing splenic function in a clinical setting, physicians should be aware of the multiple facets of spleen function (as described in Table 1) and thus the different possible approaches to determining splenic function.
In many diseases associated with splenic hypofunction such as sickle cell disease, coeliac disease, IBD and systemic lupus erythematosis, splenic function changes as the underlying disease activity alters [56, 57, 61, 64–67]. It has been suggested that these changes in splenic function are due to two components of splenic hypofunction in active disease: first, impaired splenic function, which may deteriorate during high disease activity, but may improve with treatment, and second, splenic atrophy, which may lead to irreversible loss of volume and therefore also irreversible loss of function. Illustrating this phenomenon, two patients are described in whom the size of the functional splenic tissue did not alter during relapse of the disease, causing the hyposplenia, while the clearance rate of heat-damaged autologous erythrocytes was prolonged [56, 57]. Shifts in the splenic volume-function relation can also occur in other situations, such as splenomegaly which is frequently observed in hyposplenic heterozygote sickle-cell patients . Also, hypersplenism with homogeneous organ function, splenic infarction, splenomas (regenerating nodules)  or transition to autosplenectomy can shift the splenic volume–function relation .
Because functional splenic tissue can be temporarily impaired during increased disease activity, whereas splenic atrophy is permanent, it is important to be informed about function as well as the actual volume of the organ. To measure the activity of the functional compartment of the spleen, 99mTc-labelled heat-altered autologous erythrocyte scintigraphy with quantification of spleen uptake seems the most appropriate technique. This method is well evaluated, especially in comparison with other methods . Clearance rates of 99mTc-labelled, heat-altered, autologous erythrocytes from the circulation should be considered carefully, since this is not solely dependent on splenic sequestration as the liver also partially participates in this process. Although liver uptake of 99mTc-labelled, heat-altered erythrocytes is low in controls, absolute liver uptake can vary considerably, potentially affecting secondary parameters like the spleen–liver ratio . Consequently, as the spleen is not the unique sequestering organ, with variability of liver uptake that possibly increases when splenic function is diminishing, this phenomenon may affect the axiom that measured blood clearance of cells reflects pure spleen function. Therefore, assessment of pure splenic uptake in function of the administered dose might be a better strategy.
Performing 99mTc-labelled, heat-altered erythrocyte scintigraphy on state-of-the-art SPECT-CT gamma cameras will enable the combination of both function and anatomy (volume) within a single investigation with the possibility of accounting for the exact organ volume and the volume of functional organ tissue within the organ.
The large amount of potential hyposplenic patients (Table 3) makes it almost impossible to evaluate splenic function by means of scintigraphy in every patient. Laborious preparation (cell isolation, denaturation and labelling), gamma (SPECT/CT) camera availability and even the radiation burden—albeit low—requires selection of patients eligible for this advanced technique. To screen a large group of potential hyposplenic patients, a more economical, simple and easily accessible method without radiation burden is needed. An alternative is counting the percentage of pitted erythrocytes, which is also well evaluated [22–25, 60]. It is quick, cheap and non-invasive. However, interference phase microscopy needs to be available as well as trained personnel. It should also be considered that erythrocyte pits may be heterogeneous with regard to their origin, composition, or removal kinetics . Percentages indicating hyposplenism may therefore be different in individuals who are hyposplenic for various reasons. Detection of Howell–Jolly bodies does not seem to be a reliable method of evaluating splenic function, as correlation with other methods is poor . However, measuring the percentage of Howell–Jolly bodies via flow cytometry is a potentially more reliable parameter as large amounts of erythrocytes can be screened . The percentage of argyrophilic inclusion-positive erythrocytes is a parameter that is simple and seems reliable . Measuring the percentages of both Howell–Jolly bodies by flow cytometry as well as argyrophilic inclusion-positive erythrocytes does not require special equipment. However, both methods require extensive validation. More studies evaluating the value of potentially new (immunological) markers are needed. Measuring the amount of IgM memory B cells seems a promising method, giving the opportunity to measure the susceptibility to infection in a more direct way [31, 37, 63]. Until these new methods have been validated, quantification of the percentages of pitted erythrocytes seems most reliable to screen for potential hyposplenic patients. Abnormal readings can subsequently be confirmed by scintigraphy.
Large studies comparing all available methods in various patient populations with splenic hypofunction are lacking, and data on sensitivity and specificity are scarce. To measure splenic function accurately it is important to have knowledge about the volume and function of the active splenic tissue as well as the volume of the organ itself. Function in splenic tissue can temporarily be decreased because of increased disease activity, while the spleen might actually still be partially functioning and is not in state of atrophy. Assessment of spleen function using 99mTc-labelled, heat-altered, autologous erythrocyte scintigraphy combined with a multimodality SPECT-CT approach seems best for this purpose as all facets of splenic function are evaluated. Measuring the clearance rates of 99mTc-labelled, heat-altered, autologous erythrocytes from the circulation should be considered carefully as a method of assessing splenic function, since this is not solely dependent on spleen activity.
The population of hyposplenic patients is too large to screen by the use of scintigraphy as a first-line investigation. Therefore, a cheaper, simpler, more accessible method is necessary. At present, we recommend using the percentage of pitted erythrocytes for this purpose, and refer patients with abnormal percentages for scintigraphy. Finally, more studies evaluating the value of potentially new (immunological) markers are needed.
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