TY - JOUR
T1 - T Cell Responsiveness Correlates Differentially with Antibody Isotype Levels in Clinical and Asymptomatic Filariasis
AU - Yazdanbakhsh, Maria
AU - Paxton, William A.
AU - Kruize, Yvonne C.M.
AU - Sartono, Erliyani
AU - Kurniawan, Agnes
AU - Wout van het, Angelique
AU - Selkirk, Murray E.
AU - Partono, Felix
AU - Maizels, Rick M.
AU - Yazdanbakhsh, Maria
AU - Paxton, William A.
AU - Kruize, Yvonne C.M.
AU - Sartono, Erliyani
AU - Kurniawan, Agnes
AU - Wout van het, Angelique
AU - Selkirk, Murray E.
AU - Partono, Felix
AU - Maizels, Rick M.
AU - Yazdanbakhsh, Maria
AU - Paxton, William A.
AU - Kruize, Yvonne C.M.
AU - Sartono, Erliyani
AU - Kurniawan, Agnes
AU - Wout van het, Angelique
AU - Selkirk, Murray E.
AU - Partono, Felix
AU - Maizels, Rick M.
N1 - Funding Information:
Received 19 June 1992; revised 30 November 1992. Informed consent was obtained from all patients before clinical and parasitologic study and blood withdrawal in accordance with the guidelines of Indonesian Department of Health and Human services. Grant support: EC-STD2 programme (TS2-0141-NL); De Drie Lichten Fund. Reprints or correspondence: Dr. Maria Yazdanbakhsh, Dept. ofParasito1ogy. Leiden University. Wassenaarseweg 62. Postbus 9605. 2300 RC Leiden. Netherlands.
PY - 1993/4/1
Y1 - 1993/4/1
N2 - To establish the relationships among T and B cell responses, active infection, and clinical manifestations in lymphatic filariasis, filarial-specific lymphocyte proliferation, IgG antibody isotypes, and IgE levels were determined in an exposed population: 31 asymptomatic amicrofilaremics, 43 microfilaremics, 12 symptomatic amicrofilaremics, and 52 elephantiasis patients. Lymphocyte proliferation was higher in elephantiasis patients and asymptomatic amicrofilaremics than in microfilaremics (P <.004). A proportion of asymptomatic amicrofilaremics (32%), elephantiasis patients (37%), and symptomatic amicrofilaremics (58%) showed antigen-specific lymphocyte unresponsiveness, and lymphocyte proliferation to filarial antigens correlated negatively with specific IgG41eveis (ρ = -0.315, P <.001). As elevated specific IgG4 is an indicator of active infection, it is argued that active infection may result in lymphocyte hypo responsiveness irrespective of clinical category. Ofthose with elevated specific IgE levels and high T cell proliferative responses, 70% had elephantiasis, suggesting these factors have a role in pathology. However, the existence of a proportion of elephantiasis patients with low anti-filarial IgE and T cell unresponsiveness to filarial antigens suggests that elephantiasis can be caused by distinct processes.
AB - To establish the relationships among T and B cell responses, active infection, and clinical manifestations in lymphatic filariasis, filarial-specific lymphocyte proliferation, IgG antibody isotypes, and IgE levels were determined in an exposed population: 31 asymptomatic amicrofilaremics, 43 microfilaremics, 12 symptomatic amicrofilaremics, and 52 elephantiasis patients. Lymphocyte proliferation was higher in elephantiasis patients and asymptomatic amicrofilaremics than in microfilaremics (P <.004). A proportion of asymptomatic amicrofilaremics (32%), elephantiasis patients (37%), and symptomatic amicrofilaremics (58%) showed antigen-specific lymphocyte unresponsiveness, and lymphocyte proliferation to filarial antigens correlated negatively with specific IgG41eveis (ρ = -0.315, P <.001). As elevated specific IgG4 is an indicator of active infection, it is argued that active infection may result in lymphocyte hypo responsiveness irrespective of clinical category. Ofthose with elevated specific IgE levels and high T cell proliferative responses, 70% had elephantiasis, suggesting these factors have a role in pathology. However, the existence of a proportion of elephantiasis patients with low anti-filarial IgE and T cell unresponsiveness to filarial antigens suggests that elephantiasis can be caused by distinct processes.
UR - http://www.scopus.com/inward/record.url?scp=0027513740&partnerID=8YFLogxK
U2 - 10.1093/infdis/167.4.925
DO - 10.1093/infdis/167.4.925
M3 - Article
C2 - 8450257
AN - SCOPUS:0027513740
SN - 0022-1899
VL - 167
SP - 925
EP - 931
JO - Journal of Infectious Diseases
JF - Journal of Infectious Diseases
IS - 4
ER -