Gruendl Stefanie, Matiasek Kaspar, Matiasek Lara, Fischer Andrea, Felten Sandra, Jurina Konrad, Hartmann Katrin
1 Clinic of Small Animal Medicine, Centre for Clinical Veterinary Medicine, Ludwig-Maximilians-Universitaet, Munich, Germany.
2 Section of Clinical and Comparative Neuropathology, Centre for Clinical Veterinary Medicine, Ludwig-Maximilians-Universitaet, Munich, Germany.
J Feline Med Surg. 2017 Jun;19(6):576-585. doi: 10.1177/1098612X16640839. Epub 2016 Apr 19.
Objectives The aim of the study was to evaluate whether an ante-mortem diagnosis of central nervous system (CNS) feline infectious peritonitis (FIP) is possible via immunocytochemical staining (ICC) of feline coronavirus antigen (FCoV) within macrophages of cerebrospinal fluid (CSF). Methods Prospectively, CSF samples of 41 cats were investigated, including cats with histopathologically confirmed FIP and neurological signs (n = 10), cats with confirmed FIP without CNS involvement (n = 11), cats with neurological signs but another confirmed CNS disease (n = 17), and cats without neurological signs and a disease other than FIP (n = 3). ICC staining of CSF macrophages was performed in all cats. Sensitivity, specificity, positive (PPV) and negative predictive values (NPV) of CSF ICC were calculated. Results Of 10 samples from cats with CNS FIP, eight had detectable CSF macrophages, seven of which were positive for FCoV. Ten of 11 samples from cats with confirmed FIP without neurological signs had macrophages in the CSF, with all 10 being ICC-positive. In cats with other CNS disorders, 11/17 had macrophages, two of which stained positively. In cats with diseases other than FIP and without neurological disorders, 2/3 revealed macrophages, with one cat showing positive ICC staining. Diagnosis of FIP via CSF ICC had a sensitivity of 85.0% and a specificity of 83.3%. PPV and NPV were 85.0% and 83.3%. Conclusions and relevance CSF ICC is a highly sensitive test for ante-mortem diagnosis of FIP manifesting in the CNS. However, CNS ICC specificity is too low to confirm FIP and the method should only be applied in conjunction with other features such as CSF cytology. CNS ICC could be helpful to discover pre-neurological stages of CNS FIP.
目的 本研究旨在评估通过对脑脊液(CSF)巨噬细胞内猫冠状病毒抗原(FCoV)进行免疫细胞化学染色(ICC),是否能够在生前诊断中枢神经系统(CNS)猫传染性腹膜炎(FIP)。方法 前瞻性地对41只猫的脑脊液样本进行研究,包括组织病理学确诊为FIP且有神经症状的猫(n = 10)、确诊为FIP但无CNS受累的猫(n = 11)、有神经症状但确诊为其他CNS疾病的猫(n = 17)以及无神经症状且患有FIP以外其他疾病的猫(n = 3)。对所有猫进行脑脊液巨噬细胞的ICC染色。计算脑脊液ICC的敏感性、特异性、阳性预测值(PPV)和阴性预测值(NPV)。结果 在10例患有中枢神经系统FIP的猫的样本中,8例有可检测到的脑脊液巨噬细胞,其中7例FCoV呈阳性。11例确诊为FIP但无神经症状的猫的样本中,10例脑脊液中有巨噬细胞,且全部10例ICC呈阳性。在患有其他中枢神经系统疾病的猫中,11/17有巨噬细胞,其中2例染色呈阳性。在患有FIP以外其他疾病且无神经疾病的猫中,2/3有巨噬细胞,其中1只猫ICC染色呈阳性。通过脑脊液ICC诊断FIP的敏感性为85.0%,特异性为83.3%。PPV和NPV分别为85.0%和83.3%。结论及相关性 脑脊液ICC是对中枢神经系统表现的FIP进行生前诊断的高度敏感检测方法。然而,中枢神经系统ICC特异性过低,无法确诊FIP,该方法应仅与其他特征(如脑脊液细胞学)结合应用。中枢神经系统ICC有助于发现中枢神经系统FIP的神经前期阶段。